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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046356Generated: October 26, 2026

Water → (3-Methanesulfonylphenyl)methanol

https://huagongshe.com/reaction/1046356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(Methylsulfonyl)benzaldehydeHCID 13596602—
SolventEthanolHCID 702—
Product(3-Methanesulfonylphenyl)methanolHCID 23549738—

Reaction Steps

NaBH4 is added to a solution of 750 mg (4.08 mmol) 3-methanesulphonyl-benzaldehyde in 20 ml ethanol (see P. L. Ornstein, T. J. Bleisch, M. B. Arnold, R. A. Wright, B. G. Johnson, J. P. Tizzano, D. R. Helton, M. J. Kallman, D. D. Schoepp, M. Herin, J. Med. Chem. 1998, 41(3), 358-378 or B. Eistert, W. Schade, H. Selzer, Ber. 1964, 97(5), 1470-81). The reaction mixture is stirred at room temperature for 1 h. The reaction mixture is poured into water and extracted three times with ethyl acetate. The combined organic layers are washed with water and brine, dried, filtered and concentrated in vacuo to afford the title compound, used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569317B2
Source datasetuspto-grants-2013_10
ORD IDord-d4b5f717059e41d6a68257688faed29d
Source noteuspto-grants-2013_10