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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842008Generated: October 29, 2026

Sodium borohydride → 4-Chloro-2,6-dimethylbenzyl alcohol

https://huagongshe.com/reaction/842008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18406975HCID 18406975—
SolventMethanolHCID 887—
Product4-Chloro-2,6-dimethylbenzyl alcoholHCID 69545701—

Reaction Conditions

Temperature0 °C

Reaction Steps

Dissolve 4-chloro-2,6-dimethyl benzaldehyde (5.0 g, 168.64 g/mol) in 100 mL dry methanol. Cool to 0° C. while stirring under N2. Portionwise add powdered NaBH4 (0.76g, 37.85 g/mol) over 5 minutes. Stir at 0° C. for 2 hours, monitoring by TLC until aldehyde consumed, then evaporate to a yellow oil. Add H2O (50 mL) and bring to pH. 7.0 by addition of saturated NH4Cl. Extract the neutral aqueous layer with CH2Cl2 (3×75 mL) and dry the pooled organic layers over Na2SO4. Filter and concentrate to a yellow oil. Flush through a pad of silica to remove baseline material, then evaporate to a yellow solid (3.0 g) which can be used without further purification. LCMS=171.6 (MH+), 169.6 (M−)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372743B1
Source datasetuspto-grants-2002_04
ORD IDord-8a9ea758d80142898e4d4bb121c89fc1
Source noteuspto-grants-2002_04