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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644701Generated: October 30, 2026

2-(phenylsulfonyl)benzaldehyde → HCID 59350822, compound

https://huagongshe.com/reaction/1644701

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(phenylsulfonyl)benzaldehydeHCID 640916—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 59350822HCID 5935082297.2%

Reaction Steps

Sodium borohydride (690 mg, 18.2 mmol) was added to a solution of 2-(benzenesulfonyl)-benzaldehyde (1.98 g, 8.04 mmol) and methanol (50 mL). The reaction mixture was stirred at room temperature. When vigorous bubbling subsided, the reaction mixture was cooled in an ice-water bath, then carefully quenched with a 1.0 N aqueous solution of HCl (20 mL). The mixture was concentrated to remove methanol, then the residue was diluted with water and extracted three times with ethyl acetate. The combined organic phases were dried over MgSO4, filtered, and concentrated to afford 1.94 g (97%) of (2-benzenesulfonyl-phenyl)-methanol as an oil. This product was used in subsequent steps without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124629B2
Source datasetuspto-grants-2012_02
ORD IDord-136e7dbaf7f648a4976879b2dabb8d7f
Source noteuspto-grants-2012_02