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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266965Generated: October 26, 2026

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

https://huagongshe.com/reaction/266965

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 Conditions

Temperature10 °C

Reaction Steps

To a flask charged with sodium borohydride (1.5 g, 39.4 mmol) under nitrogen and chilled to 10° C. was added, slowly, a solution of 1-[4-(3-chloropropoxy)-3-hydroxyphenyl]ethanone (6.0 g, 26.2 mmol) 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, 5.3 mmol) 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 numberUS05652241
Source datasetuspto-grants-1997_07
ORD IDord-31f3dbe075f64b1c84f3ed08cab09e1e
Source noteuspto-grants-1997_07