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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217697Generated: October 29, 2026

3-(3-Hydroxyprop-1-ynyl)-N-phenylbenzenesulfonamide → 3-(3-Oxoprop-1-ynyl)-N-phenylbenzenesulfonamide

https://huagongshe.com/reaction/2217697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-Hydroxyprop-1-ynyl)-N-phenylbenzenesulfonamideHCID 22492482—
SolventDichloromethaneHCID 6344—
SolventTriacetoxyperiodinaneHCID 159087—
Product3-(3-Oxoprop-1-ynyl)-N-phenylbenzenesulfonamideHCID 2249246486.7%

Reaction Steps

3-(3-Hydroxyprop-1-ynyl)-N-phenylbenzenesulfonamide (53a) (0.55 g, 1.9 mmol) was dissolved in a solution of Dess-Martin reagent in methylene chloride (0.157 g/ml) (8.2 ml) and the resultant mixture was stirred at ambient temperature for 30 min. The mixture was partitioned between water (50 ml) and ether (50 ml), and ether solution was washed successively with 5% Na2CO3, water, and dried (Na2SO4). The solvents were removed under reduced pressure to give the title compound (0.47 g, 72%) as an oil. The crude product 54a was used in the further step without an additional purification. 1H NMR (DMSO-d6, HMDSO) δ: 6.96-7.41 (5H, m, C6H5); 7.54-8.07 (4H, m, C6H4); 9.45 (1H, s, CH); 10.41 (1H, s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407988B2
Source datasetuspto-grants-2008_08
ORD IDord-4625cfe9c7c74da1980a191d6ed9cec9
Source noteuspto-grants-2008_08