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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106649Generated: November 1, 2026

Tert-Butyl nitrite → Thionitrous acid (HNOS), S-(triphenylmethyl) ester

https://huagongshe.com/reaction/1106649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
ReactantBenzenemethanethiol, alpha,alpha-diphenyl-HCID 77281—
SolventDichloromethaneHCID 6344—
ProductThionitrous acid (HNOS), S-(triphenylmethyl) esterHCID 9518698.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphenylmethyl mercaptan (0.050 g, 0.18 mmol) was dissolved in anhydrous methylene chloride and cooled to 0° C. Tert-butyl nitrite (0.186 g, 1.80 mmol) was added and the resulting mixture was stirred at 0° C. for 30 min. The reaction mixture was allowed to warm to room temperature and stirred at room temperature for 1 hour. The solvent and excess of tert-butyl nitrite were evaporated to give the title compound as a green solid (0.054 g, 98%). 1H NMR (CDCl3) δ: 7.13-7.18 (m, 4 H), 7.25-7.39 (m, 11 UH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057347
Source datasetuspto-grants-2000_05
ORD IDord-e41ae4de196a414b9e7310e7c629bddf
Source noteuspto-grants-2000_05