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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443746Generated: October 29, 2026

Pyridine → Isopropyl (chlorosulfinyl)(phenyl)carbamate

https://huagongshe.com/reaction/443746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantProphamHCID 24685—
SolventTetrahydrofuranHCID 8028—
ProductIsopropyl (chlorosulfinyl)(phenyl)carbamateHCID 1272880761.1%

Reaction Steps

Eighteen grams isopropyl phenylcarbamate (~0.1 mol) and 14.0 g thionyl chloride (0.12 mol) were dissolved in 50 ml dry tetrahydrofuran and protected from moisture by a calcium chloride tube. Eight grams pyridine (0.1 mol) were added dropwise while the mixture was stirring at a water bath temperature (15°-20° C.). After the addition of pyridine was completed, the mixture was stirred for 12 hours at room temperature. Pyridine hydrochloride was filtered and the solvent was removed under vacuum. The concentrated residue was diluted with hexane and filtered. The hexane was removed under vacuum and the residue was distilled, giving 16.0 g of product distilling at 113-115/0.08 mm. NMR spectrum of the product in chloroform-d-TMS gave the following absorptions: δ7.6-7.2 (m, 5H, phenyl protons), δ5.5-4.9 (m, 1H, CH) and δ1.4-1.3 (d, 6H, C(CH3)2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261897
Source datasetuspto-grants-1981_04
ORD IDord-bf312fb42f2541cb8fb0654ff628516a
Source noteuspto-grants-1981_04