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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235387Generated: October 31, 2026

Sodium borohydride → HCID 67427396, compound

https://huagongshe.com/reaction/2235387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Difluoro-4-isopropoxybenzaldehydeHCID 79111183—
SolventEthanolHCID 702—
ProductHCID 67427396HCID 67427396—

Reaction Steps

To a suspension of 3,5-difluoro-4-isopropoxy-benzaldehyde (0.14 g) in EtOH (10 ml) is added NaBH4 (60.7 mg; 1.61 mmol) at 10° C. in 5 portions. The mixture is slowly warmed to RT and stirred for 3 h. After aqueous work-up (3,5-difluoro-4-isopropoxy-phenyl)-methanol is obtained which is directly chlorinated using SOCl2 (1 ml; 13.8 mmol) in CH2Cl2 (10 ml) at RT for 3 h. After aqueous work-up 5-chloromethyl-1,3-difluoro-2-isopropoxy-benzene (0.14 g) is obtained as a yellow oil which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714010B2
Source datasetuspto-grants-2010_05
ORD IDord-dc6dfce5dea547899a928ecc392aa07a
Source noteuspto-grants-2010_05