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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351080Generated: October 31, 2026

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

https://huagongshe.com/reaction/351080

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 numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-b789970a94b84fe8b0d3c3e7f530fde8
Source noteuspto-grants-2007_02