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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071083Generated: October 30, 2026

Trimethyl borate → HCID 68670785, compound

https://huagongshe.com/reaction/2071083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
Reactant1,3-Dibromo-5-(dimethoxymethyl)benzeneHCID 19093458—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68670785HCID 6867078545.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirring solution of 23 mL of n-BuLi (1.6 M in hexanes) in 20 mL of THF at −78° C. was added 5.31 g of 1,3-dibromo-5-(dimethoxymethyl)benzene in 80 mL of THF dropwise over a period of about 55 min. After 50 min., 3.2 mL (28.7 mmol) of B(OMe)3 was added, and the solution was stirred at −78° C. for 20 min. The cold bath was removed and stirring continued with gradual warming to r.t. After 1 h, 1 N HCl (45 mL) was added, and the aqueous layer was extracted with EtOAc. The extract was washed with brine, dried over Na2SO4, filtered, and concentrated. To a stirring mixture of crude product in 70 mL of 1N NaOH at 0° C. was added 14.5 mL of H2O2 (30 wt % in H2O) dropwise. After 25 min., 5 N HCl was added to a pH=1, and EtOAc and H2O were added. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (15% EtOAc/hexanes) provided 1.92 g of 3-bromo-5-(dimethoxymethyl)phenol as a pale yellow solid with some impurity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-d1c590ecffec4775abad674201727e62
Source noteuspto-grants-2012_10