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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185369Generated: October 30, 2026

Sodium borohydride → 4-Hydroxymethyl-3-isopropyl-phenyl 1,1,1-trifluoro-methanesulfonate

https://huagongshe.com/reaction/2185369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Formyl-3-isopropyl-phenyl 1,1,1-trifluoro-methanesulfonateHCID 22568910—
SolventMethanolHCID 887—
Product4-Hydroxymethyl-3-isopropyl-phenyl 1,1,1-trifluoro-methanesulfonateHCID 22568893—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-formyl-3-isopropyl-phenyl 1,1,1-trifluoro-methansulfonate (Intermediate 148, 540.0 mg, 1.82 mmols) in 7 mL MeOH at 0° C. was added NaBH4 (72.0 mg, 1.91 mmols). After stirring 2 hours at 0° C. the reaction was carefully quenched with H2O and extracted with Et2O. The combined organic layers were washed with H2O and saturated aqueous NaCl, dried (MgSO4), and concentrated under reduced pressure. The title compound was isolated by column chromatography (5-10% EtOAc-hexanes) as a colorless oil, 355.0 mg (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399774B1
Source datasetuspto-grants-2002_06
ORD IDord-dbf0c4822b8549baafa1002c29217527
Source noteuspto-grants-2002_06