1-(tert-Butoxycarbonyl)-1,4,5,6-tetrahydropyridin-2-ylboronic acid pinacol ester

Product Number: B14416; CAS Number: 865245-32-5

B14416 Technical Data Sheet

SDS

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1-(tert-Butoxycarbonyl)-1,4,5,6-tetrahydropyridin-2-ylboronic acid pinacol ester tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate CAS: 865245-32-5 MDL: MFCD07776601

Molecular weight: 309.2 g/mol

Molecular Formula: C16H28BNO4

CAS Number: 865245-32-5

Storage: Store at 2-8 Co, under dry conditions.

Synonyms:   tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate, tert-butyl 6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4, tetrahydropyridine-1-carboxylate, 1-Boc-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1,2,3,4-tetrahydropyridine, 1-Boc-1,4,5,6-tetrahydropyridine-2-boronic Acid Pinacol Ester, tert-butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-pyridine-1-carboxylate, (1-(TERT-BUTOXYCARBONYL)-1,4,5,6-TETRAHYDROPYRIDIN-2-YL)BORONIC ACID PINACOL ESTER

Uses: Synthesis building block, Organic Synthesis, Transition Metal Coupling

1-(tert-Butoxycarbonyl)-1,4,5,6-tetrahydropyridin-2- ylboronic acid pinacol ester, is a synthetic specialty chemical useful in the synthesis of pharmaceuticals and fine organic chemicals.

Pinacol Ester Derivative Coupling Reactions

1.) Palladium(0)-Catalyzed Cross-Cross-Coupling Reaction of Alkoxydiboron with Haloarenes: A Direct Procedure for Arylboronic Esters, Ishiyama, Tatsuo, Murata, Miki, Miyaura, Norio, Journal of Organic Chemistry (1995), 60(23), 7508-10. DOI:10.1021/jo00128a024

2.) Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration, Imao, Daisuke, Glasspoole, Ben W., Laberge, Veronique S., Crudden, Cathleen M., Journal of the American Chemical Society (2009), 131(14), 5024-5025. DOI:10.1021/ja8094075

3.) Palladium-Catalyzed Cross-Coupling Reaction of Bis(pinacolato)diboron with 1-Alkenyl Halides or Triflates: Convenient Synthesis of Unsymmetrical 1,3-Dienes via the Borylation-Coupling Sequence, Takagi, Jun, Takahashi, Kou, Ishiyama, Tatsuo, Miyaura, Norio, Journal of the American Chemical Society (2002), 124(27), 8001-8006. DOI:10.1021/ja0202255

4.) Functionalized olefin cross-coupling to construct carbon-carbon bonds, Lo, Julian C., Gui, Jinghan, Yabe, Yuki, Pan, Chung-Mao, Baran, Phil S., Nature (London, United Kingdom) (2014), 516(7531), 343-348. DOI:10.1038/nature14006.

5.) The Synthesis of Highly Substituted Isoxazoles by Electrophilic Cyclization: An Efficient Synthesis of Valdecoxib, Waldo, Jesse P., Larock, Richard C., Journal of Organic Chemistry (2007), 72(25), 9643-9647. DOI:10.1021/jo701942e.

6.) Arenes to anilines and aryl ethers by sequential iridium-catalyzed borylation and copper-catalyzed coupling, Tzschucke, C. Christoph, Murphy, Jaclyn M., Hartwig, John F., Organic Letters (2007), 9(5), 761-764. DOI:10.1021/ol062902w

7.) A synthesis of allyboronates via the palladium(0)-catalyzed cross-coupling reaction of bis(pinacolato)diboron with allylic acetates, Ishiyama, Tatsuo, Ahiko, Taka-aki, Miyaura, Norio, Tetrahedron Letters (1996), 37(38), 6889-6892. DOI:10.1016/0040-4039(96)01505-5

8.) Rapid synthesis of 3-amino-imidazopyridines by a microwave-assisted four-component coupling in one pot, DiMauro, Erin F., Kennedy, Joseph M., Journal of Organic Chemistry (2007), 72(3), 1013-1016, DOI:10.1021/jo0622072

9.) Iron-Catalyzed C(sp2)-H Bond Functionalization with Organoboron Compounds, Shang, Rui, Ilies, Laurean, Asako, Sobi, Nakamura, Eiichi, Journal of the American Chemical Society (2014), 136(41), 14349-14352. DOI:10.1021/ja5070763

10.) Copper-Promoted Coupling of Vinyl Boronates and Alcohols: A Mild Synthesis of Allyl Vinyl Ethers, Shade, Ryan E., Hyde, Alan M., Olsen, John-Carl, Merlic, Craig A., Journal of the American Chemical Society (2010), 132(4), 1202-1203. DOI:10.1021/ja907982w

SDS

Categories

Organoborons

Scaffold/Subcategory

Boronic Ester

CAS #

[865245-32-5]

Purity %

97%

Smiles

CC(C)(C)OC(=O)N1CCCC=C1B1OC(C)(C)C(C)(C)O1

Molecular Weight

309.21

Molecular Formula

C16H28BNO4

Functional Groups

Nitrogen Heterocycle

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