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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856691Generated: October 31, 2026

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

https://huagongshe.com/reaction/1856691

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)propanoic acid, ethyl ester (7.5 g, Example 15a)) in ethanol (20 ml) at 5° C. The resulting solution was allowed to warm to room temperature and was stirred for 10 hours before being concentrated under reduced pressure. The residue was partitioned between ethyl acetate (100 ml) and 2N 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 numberUS06143751
Source datasetuspto-grants-2000_11
ORD IDord-d0e92b8121e74b38b07ba4b07dee9bf9
Source noteuspto-grants-2000_11