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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358758Generated: October 31, 2026

Sodium borohydride → [3-(4-Chloro-2-nitro-phenoxy)-phenyl]-methanol

https://huagongshe.com/reaction/2358758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-Chloro-2-nitro-phenoxy)-benzaldehydeHCID 9281341—
SolventEthanolHCID 702—
Product[3-(4-Chloro-2-nitro-phenoxy)-phenyl]-methanolHCID 6845670694.4%

Reaction Steps

To the product from Example 176a (2.0 g. 7.2 mmol) in ethanol (25 mL) was added sodium borohydride (0.32 g, 8.6 mmol). The reaction was stirred for 4 h. The excess sodium borohydride was destroyed by the addition of acetic acid. The reaction was poured into water and extracted with ethyl acetate. The organic layer was separated and washed with water, brine, and dried over sodium sulfate, filtered and concentrated under vacuum giving the title compound (1.9 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763731B2
Source datasetuspto-grants-2010_07
ORD IDord-d029e69cdf354ed4bb35c5a3e02602f6
Source noteuspto-grants-2010_07