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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186995Generated: October 31, 2026

Lithium borohydride → 2-(2-Chloro-4-cyano-5-methoxyphenyl)ethanol

https://huagongshe.com/reaction/1186995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantMethyl (2-chloro-4-cyano-5-methoxyphenyl)acetateHCID 77231255—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chloro-4-cyano-5-methoxyphenyl)ethanolHCID 66644009—

Reaction Steps

To a solution of methyl(2-chloro-4-cyano-5-methoxyphenyl)acetate (200 mg, 0.835 mmol) in THF (5 mL) was added 2M lithium borohydride (0.835 mL, 1.67 mmol) and the reaction was stirred at RT for 16 hours. The reaction was diluted with ether and quenched into water containing 2N HCl. The mixture was extracted twice with ethyl acetate and the organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo. The product mixture was separated by MPLC (40+S; 20-60% ethyl acetate/hexanes) to afford the title product. 1H-NMR (400 MHz, CDCl3) δ ppm 3.04 (t, J=6.4 Hz, 2H), 3.93 (t, J=6.4 Hz, 2H), 3.93 (s, 3H), 6.927 (s, 1H), 7.536 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-2374aa201d1341cab40e3fea2b3a7f0a
Source noteuspto-grants-2014_03