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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379968Generated: October 30, 2026

Sodium borohydride → (S)-2-(4-Bromophenoxy)propan-1-ol

https://huagongshe.com/reaction/379968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(2S)-2-(4-bromophenoxy)propanoic acid, ethyl esterHCID 86756006—
SolventEthanolHCID 702—
Product(S)-2-(4-Bromophenoxy)propan-1-olHCID 57234620—

Reaction Steps

Sodium borohydride (1.15 g) was added to a solution of (2S)-2-(4-bromophenoxy)propionic acid, ethyl ester (7.5 g, Example 4a)) in ethanol (20 ml) at 5° C. The resulting solution was allowed to attain room temperature and was stirred for 10 hours before being concentrated under reduced pressure. The residue was partitioned between ethyl acetate (100 ml) and 2M hydrochloric acid (50 ml). The mixture was extracted into ethyl acetate and the combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The product was used directly in the next step without further purification (6.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300352B1
Source datasetuspto-grants-2001_10
ORD IDord-d38eb53027f6405ba51c2be9abe29780
Source noteuspto-grants-2001_10