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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197922Generated: October 31, 2026

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

https://huagongshe.com/reaction/2197922

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 numberUS08338605B2
Source datasetuspto-grants-2012_12
ORD IDord-1165335a63734cfa82a802118e0fdd81
Source noteuspto-grants-2012_12