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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469190Generated: November 2, 2026

Methanol → (5-Bromo-2-chlorothiophen-3-yl)methanol

https://huagongshe.com/reaction/1469190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
Reactant5-Bromo-2-chlorothiophene-3-carboxylic acidHCID 22397190—
SolventTetrahydrofuranHCID 8028—
Product(5-Bromo-2-chlorothiophen-3-yl)methanolHCID 2307016099.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of acid 1 (3.0 g, 12.4 mmol) in THF (50 mL) were added borane dimethylsulfide complex (10M in THF, 3.2 mL, 31.1 mmol) at 0° C. The mixture was stirred at 0° C. for 15 min, at room temperature for 45 min, and at 65° C. for 2 hours. The reaction mixture was cooled to 0° C. To the mixture were added MeOH (30 mL), H2O (250 mL) dropwise at 0° C. The mixture was extracted with EtOAc (100 mL). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to obtain the title compound 31 (2.8 g, 99%). The crude alcohol 31 was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006187B2
Source datasetuspto-grants-2015_04
ORD IDord-adf4f30a26f14787a65a0f0c1462f7b0
Source noteuspto-grants-2015_04