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704415

Sigma-Aldrich

Vinylboronic acid MIDA ester

97%

Synonym(s):

6-Methyl-2-vinyl-1,3,6,2-dioxazaborocane-4,8-dione

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1 G
$102.81
5 G
$280.00
25 G
$952.00

About This Item

Empirical Formula (Hill Notation):
C7H10BNO4
CAS Number:
1104636-73-8
Molecular Weight:
182.97
MDL number:
MFCD11656092
UNSPSC Code:
12352103
PubChem Substance ID:
329762451
NACRES:
NA.22

$102.81

List Price$129.00Save 20%
Web-Only Promotion

Available to ship onApril 22, 2025Details

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Quality Level

100

assay

97%

form

powder

mp

152-156 °C

storage temp.

2-8°C

SMILES string

CN1CC(=O)OB(OC(=O)C1)C=C

InChI

1S/C7H10BNO4/c1-3-8-12-6(10)4-9(2)5-7(11)13-8/h3H,1,4-5H2,2H3

InChI key

MGRQGYAVASCCAK-UHFFFAOYSA-N

Related Categories

General description

Vinylboronic acid MIDA ester, like other MIDA boronates, possesses the capacity for controlled, in situ slow-release of boronic acids under aqueous basic conditions allowing the cross-coupling of classically challenging substrates.[1][2]

Application

MIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings

Suzuki Cross-Coupling with MIDA Boronates
  • Vinylboronic acid MIDA ester is an air and chromatographically stable boronic acid surrogate for Suzuki-Miyaura cross-coupling. It can also be used in Heck and oxidative Heck reactions as well as in olefin metathesis to provide the cross-coupled product.[1][2]
  • It is compatible with a wide range of common synthetic reagents that allows functionalization to synthesize structurally complex boronic acid surrogates.[1][3]
  • It undergoes cyclopropanation and epoxidation to yield corresponding MIDA cyclopropane and oxirane, respectively.[3][4][5]
  • It can be used as one of the major reagents for the scalable synthesis of potent cytotoxin, Leiodermatolide[6] and for the total synthesis of (−)-Blepharocalyxin D.[7]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP2460
SHBL0979
SHBK3494
SHBH2828V
SHBG6869V

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Total Synthesis of (−)-Blepharocalyxin D and Analogues.
Cons BD, et al.
Organic Letters, 15(8), 2046-2049 (2013)
A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.
Knapp DM, et al.
Journal of the American Chemical Society, 131(20), 6961-6963 (2009)
(1-Bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.
Woerly EM, et al.
Tetrahedron, 69(36), 7732-7740 (2013)
Synthesis of trans-2-(Trifluoromethyl) cyclopropanes via Suzuki reactions with an N-methyliminodiacetic acid boronate.
Duncton MA and Singh R.
Organic Letters, 15(17), 4284-4287 (2013)
Vinyl MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.
Uno BE, et al.
Tetrahedron, 65(16), 3130-3138 (2009)
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