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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735700Generated: October 29, 2026

1-(4-Bromophenyl)propan-2-one → 1-(4-Bromophenyl)propan-2-ol

https://huagongshe.com/reaction/735700

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)propan-2-oneHCID 736332—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product1-(4-Bromophenyl)propan-2-olHCID 1988290196.9%

Reaction Steps

To a solution of 4-bromophenylacetone (5.00 g, 23.5 mmol) in ethanol (100 mL) at 0° C., was added sodium borohydride (976 mg, 25.8 mmol) portionwise over 5 min. The mixture was stirred at rt for 15 h, then quenched with 5% citric acid. The volatile solvent was removed in vacuo. The mixture was diluted with water, the pH was adjusted to 4.5 with 1N HCl, then aqueous phase was extracted with CH2Cl2 (3×). The combined organic washed with brine, dried (Na2SO4), filtered through a pad of SiO2 (eluted with 10% EtOAc/CH2Cl2) and concentrated to afford 4.90 g of 77A as a colorless oil. MS (ESI) m/z 197.1 (M-OH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592331B2
Source datasetuspto-grants-2009_09
ORD IDord-26d3f76f7853431ca54b6881610a6e64
Source noteuspto-grants-2009_09