Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658307Generated: October 29, 2026

Sodium borohydride → 4-(1-Hydroxymethyl-heptyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/658307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(1-Formyl-heptyl)-benzoic acid methyl esterHCID 86625833—
SolventEthanolHCID 702—
Product4-(1-Hydroxymethyl-heptyl)-benzoic acid methyl esterHCID 67486158—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(1-Formyl-heptyl)-benzoic acid methyl ester (3.17 g, 12.1 mmol) is dissolved in ethanol (50 mL) and allowed to stir under nitrogen in an ice bath at 0° C. Sodium borohydride (0.457 g, 12.1 mmol) is added to the mixture in one portion. The reaction is allowed to stir at 0° C. for one hour, then warmed slowly to room temperature for several hours and is monitored by TLC. Upon complete consumption of starting material, the reaction is carefully quenched with water and the ethanol is removed in vacuo. The remaining mixture is diluted with ethyl acetate. The two phases are separated, and the organic layer washed, dried, and concentrated. The title compound is used in the next step without further purification. MS (ES): 265.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076374B2
Source datasetuspto-grants-2011_12
ORD IDord-c9cb90b95655470f95d38a58a967bbc7
Source noteuspto-grants-2011_12