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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364579Generated: October 29, 2026

Hydrochloric Acid → (4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/1364579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methanesulfonyl-2-(trifluoromethyl)benzaldehydeHCID 51342018—
SolventEthanolHCID 702—
Product(4-(Methylsulfonyl)-2-(trifluoromethyl)phenyl)methanolHCID 66936507—

Reaction Steps

To a suspension of 4-methanesulfonyl-2-trifluoromethyl-benzaldehyde (49.2 g, 0.20 mol) in dry EtOH (500 ml), cooled in an ice-bath, is added sodium borohydride (10.8 g, 0.22 mol), portionwise over 30 mins. The reaction mixture is allowed to warm up slowly to room temperature then stirring is continued for 16 h. The reaction mixture is poured into a beaker of crushed ice (700 ml) and adjusted to pH 1 with 2N HCl (approx. 200 ml). The resulting pale yellow suspension is extracted with CH2Cl2 (3×150 ml), dried (MgSO4) and evaporated to dryness in vacuo. to afford a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888383B2
Source datasetuspto-grants-2011_02
ORD IDord-73aca806d3dc47a1b52b33f1efaadbaf
Source noteuspto-grants-2011_02