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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117285Generated: October 30, 2026

Acetic Acid → N-(4-Sulfanylphenyl)benzamide

https://huagongshe.com/reaction/2117285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 86610051HCID 86610051—
CatalystZincHCID 23994—
SolventDichloromethaneHCID 6344—
ProductN-(4-Sulfanylphenyl)benzamideHCID 15465270—

Reaction Steps

Benzoyl chloride (5.14 mL, 44.28 mL) was added dropwise to a mixture of 4-aminophenol disulfide (5.0 g, 20.13 mmol) and TEA (7.01 mL, 50.3 mmol) in 60 mL DCM at 0° C. The reaction was allowed to stir overnight. The resulting precipitate was collected by filtration. The solid was washed with MeOH and water and then dried. The solid was combined with 200 mL of concentrated HOAc, and 5.0 equiv of zinc powder was added. The reaction was monitored by LCMS. When the reaction was complete, the acetic acid solution was concentrated to approximately 20 mL in volume. The crude mixture was then extracted with water and EtOAc. The organic layer was dried with MgSO4 then concentrated. MS: 228 [M+H]+; 1H NMR (DMSO-d6): 10.23 (s, 1H), 7.94 (d, 2H), 7.81 (d, 2H), 7.56 (m, 3H), 7.28 (d, 2H), 5.31 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442700B2
Source datasetuspto-grants-2008_10
ORD IDord-aa195a4e81ce4680a347ac2179fd5379
Source noteuspto-grants-2008_10