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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257628Generated: November 1, 2026

Sodium borohydride → 4-(3-Chloropropoxy)-3-hydroxy-alpha-methylbenzenemethanol

https://huagongshe.com/reaction/2257628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-(4-(3-Chloropropoxy)-3-hydroxyphenyl]ethanoneHCID 10376507—
SolventTetrahydrofuran ethanolHCID 21873804—
Product4-(3-Chloropropoxy)-3-hydroxy-alpha-methylbenzenemethanolHCID 1039898655%

Reaction Steps

To a flask charged with sodium borohydride (1.5 g, 0.0394 mol) under nitrogen and chilled to 10° was added, slowly, a solution of 1-[4-(3-chloropropoxy)-3-hydroxyphenyl]ethanone (6.0 g, 0.0262 mol) dissolved in ethanol-tetrahydrofuran (120 ml, 2:1). After total addition, the ice bath was removed and the reaction was stirred at ambient temperature for 3 hours. An additional amount of sodium borohydride (0.2 g, 0.0053 mol) was carefully added. After stirring at ambient temperature for one hour, the solvent was removed in vacuo. The resultant solid residue was diluted with water (100 ml) and left overnight. The product was isolated by vacuum filtration yielding 3.8 g. Two consecutive recrystallizations from toluene provided 3.3 g (55%) of 4-(3-chloropropoxy)-3-hydroxy-α-methylbenzene methanol as a light brown solid, m.p.=107°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658911
Source datasetuspto-grants-1997_08
ORD IDord-2dbe91e873994c7ba698f61f148c97b5
Source noteuspto-grants-1997_08