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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017626Generated: October 31, 2026

Methanol → 2,3-Dichlorobenzyl alcohol

https://huagongshe.com/reaction/1017626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2,3-DichlorobenzaldehydeHCID 35745—
ReactantSodium borohydrideHCID 4311764—
SolventSodium HydroxideHCID 14798—
Product2,3-Dichlorobenzyl alcoholHCID 228603100.5%

Reaction Steps

To solution of MeOH (150 ml) containing 2,3-dichlorobenzaldehyde (20 g, 0.11 mole), cooled in ice bath, was added a solution of NaBH4 (4.54 g, 0.12 mole) in 0.2 M NaOH (15 mL) slowly over 15 min under nitrogen atmosphere. After completion of the addition, the mixture was allowed to warm up gradually to rt, and stirred for 2.5 h at rt. The reaction was quenched by cooling the mixture and pouring it slowly to ice water (˜700 mL). The mixing led to formation of white precipitates. After stirring for 30 min. the precipitates were collected on Bòcbner funnel, and the collected solid was dissolved in EtOAc (200 mL). The organic solution was washed with 0.1 M NaOH (150 mL), dried over Na2SO4, and concentrated to dryness in vacuo, yielding 2,3-dichlorobenzylalcohol as white solid (19.57 g, 97%). Rf=0.46 in EtOAc/hexane (1/3). 1H-NMR (CD3OD, 299.96 MHz: δ (ppm) 7.52-7.49 (dd, 1H), 7.45-7.42 (dd, 1H), 7.33-7.27 (t, 1H), 4.70 (s, 2H). Retention time (anal. HPLC: 10 to 70% MeCN/H2O over 6 min)=4.00 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479498B1
Source datasetuspto-grants-2002_11
ORD IDord-da51d8e7dec1499ebf6d2f0f4e124c47
Source noteuspto-grants-2002_11