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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454992Generated: October 25, 2026

Sodium Hydroxide → 3-(3-Bromophenyl)propan-1-ol

https://huagongshe.com/reaction/1454992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(3-bromophenyl)propanoic AcidHCID 2063862—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Bromophenyl)propan-1-olHCID 18785928—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 1.84 g (8 mmol) of 3-(3-bromophenyl)propionic acid and 0.91 g (24 mmol) of sodium borohydride in 20 ml of THF, cooled to 0° C., is admixed in small portions with 3.2 ml (25 mmol) of trifluoroborane-diethyl ether complex. Stirring is continued in the cold for 1 hour, and then at ambient temperature for 16 hours. The reaction mixture is cooled to 0° C. and neutralized to a pH of 7˜8 by adding a 1N solution of aqueous sodium hydroxide. It is concentrated under reduced pressure and then the residue is taken up in water. It is extracted with dichloromethane and dried over sodium sulphate. Following filtration, the organic phase is concentrated under reduced pressure. This gives 1.62 g (7.53 mmol) of product in the form of an oil, which is used as it is in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482346B2
Source datasetuspto-grants-2009_01
ORD IDord-beb07457d4e8475cbdb04a25541f093e
Source noteuspto-grants-2009_01