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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669329Generated: November 3, 2026

Sodium borohydride → 1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-ol

https://huagongshe.com/reaction/1669329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-oneHCID 67342443—
SolventEthanolHCID 702—
Product1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-olHCID 6734503394.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(4-Bromo-3-methyl-phenyl)-5-methyl-hexan-1-one (3.5 g, 12.4 mmol) was dissolved in ethanol and cooled to 0° C. while stirring under nitrogen. To the flask was added sodium borohydride (469 mg, 12.4 mmol), and the reaction was kept at 0° C. for 1 h., then slowly warmed to room temperature. The reaction was monitored by HPLC. Upon complete consumption of starting material, the reaction is carefully quenched with water, the ethanol removed by rotary evaporator, and extracted with diethyl ether, washed, dried, and concentrated. The title compound (3.33 g, 11.72 mmol), is used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-72b9b7aab46c4078a77272c2e0b35549
Source noteuspto-grants-2011_08