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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180431Generated: October 31, 2026

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

https://huagongshe.com/reaction/2180431

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 numberUS06888027B2
Source datasetuspto-grants-2005_05
ORD IDord-1f2992752a354da28ab073c1039a88a1
Source noteuspto-grants-2005_05