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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350007Generated: November 1, 2026

Hydrochloric Acid → 4-(2-Phenyl-4-thiazolylmethoxy)benzyl alcohol

https://huagongshe.com/reaction/350007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2-Phenyl-4-thiazolylmethoxy)benzaldehydeHCID 10517961—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product4-(2-Phenyl-4-thiazolylmethoxy)benzyl alcoholHCID 6888821690.1%

Reaction Steps

Sodium borohydride (0.45 g) was added to a mixture of 4-(2-phenyl-4-thiazolylmethoxy)benzaldehyde (6.35 g), tetrahydrofuran (30 ml) and methanol (20 ml) under ice-cooling, which was stirred at room temperature for 30 minutes. The reaction mixture was neutralized with dilute hydrochloric acid and water to give a precipitate, which was collected by filtration and then air-dried to obtain crystals of 4-(2-phenyl-4-thiazolylmethoxy)benzyl alcohol (5.76 g, yield 90%). This was recrystallized from ethyl acetate-hexane to obtain colorless needles. Melting point: 145–146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179823B1
Source datasetuspto-grants-2007_02
ORD IDord-654d4623bb144946b801621b4165af79
Source noteuspto-grants-2007_02