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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921874Generated: October 26, 2026

Hydrochloric Acid → 1,3-Difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzene

https://huagongshe.com/reaction/1921874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant3,5-Difluoro-4-triisopropylsilanyloxybenzaldehydeHCID 57971920—
SolventMethanolHCID 887—
Product1,3-Difluoro-5-hydroxymethyl-2-triisopropylsilanyloxybenzeneHCID 57971896—

Reaction Conditions

Temperature0 °C

Reaction Steps

35.0 g (111 mmol) of 3,5-difluoro-4-triisopropylsilanyloxybenzaldehyde are introduced into 150 ml of water and 40 ml of methanol, cooled to 0° C. and, after addition of 8.42 g (222 mmol) of sodium borohydride in portions, stirred at RT overnight. The mixture is cautiously acidified with 1 N hydrochloric acid and extracted with ethyl acetate, and the combined organic phases are washed with saturated sodium chloride solution and dried over magnesium sulfate, and the solvent is distilled out in vacuo. Chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 4:1) results in 29.5 g (93.2 mmol, 84% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173704B2
Source datasetuspto-grants-2012_05
ORD IDord-74494ef89d704db8a97c6cb4d099dcd0
Source noteuspto-grants-2012_05