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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435616Generated: October 30, 2026

5-Nitro-2-(phenylsulfanyl)benzaldehyde → [5-Nitro-2-(phenylsulfanyl)phenyl]methanol

https://huagongshe.com/reaction/435616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Nitro-2-(phenylsulfanyl)benzaldehydeHCID 2981067—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product[5-Nitro-2-(phenylsulfanyl)phenyl]methanolHCID 54372723—

Reaction Steps

450 g of 3-nitro-6-(phenylthio)-benzaldehyde are suspended in 4 litres of ethanol and treated portionwise with 111 g of sodium borohydride. The mixture is stirred for a further 6 hours. The mixture is then diluted with 4 litres of water and extracted with ether. The organic solution is washed successively with water and aqueous sodium bicarbonate solution, dried over magnesium sulphate and evaporated under reduced pressure. The crude product is recrystallised from benzene/petroleum ether. There is obtained 3-nitro-6-(phenylthio)-benzyl alcohol of melting point 104°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006145
Source datasetuspto-grants-1977_02
ORD IDord-4b8c419171db43af8d23c23e884b0e6e
Source noteuspto-grants-1977_02