Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598845Generated: October 26, 2026

Trimethyl borate → [6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]boronic acid

https://huagongshe.com/reaction/1598845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-6-(4-fluorophenyl)-1,3-benzodioxoleHCID 23451068—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[6-(4-Fluorophenyl)-1,3-benzodioxol-5-yl]boronic acidHCID 2345119950%

Reaction Steps

Under nitrogen, 6.3 mL (15.8 mmol) of n-BuLi (2.5M in hexanes) was added to a stirred solution of 3.9 g (13.2 mmol) of 5-bromo-6-(4-fluorophenyl)-1,3-benzodioxole (Step 1) in 30 mL of anhydrous THF at -78° C. After 30 minutes, 4.5 mL (39.4 mmol) of trimethylborate was added. The reaction was warmed to ambient temperature and stirred for 3 hours prior to the addition of 60 mL of 5% NaOH. The reaction was stirred for an additional 60 minutes, the THF removed in vacuo, and the pH adjusted to ca. 4. The residue was dissolved in ethyl acetate; the resulting solution was dried over Na2S04 and concentrated in vacuo to give 1.7 g (50%) of [6 (4-fluorophenyl)-1,3-benzodioxol-5-yl] boronic acid as a pale yellow solid: NMR (CDCl3) δ 4.00 (br s, 2H), 6.06 (s, 2H), 6.75 (s, 1H), 7.08-7.17 (m, 2H), 7.26 (s, 1H), 7.31-7.39 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739166
Source datasetuspto-grants-1998_04
ORD IDord-3c89c5b136084f87820630f7ac0e21ad
Source noteuspto-grants-1998_04