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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336196Generated: October 29, 2026

Toluene → 1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chloride

https://huagongshe.com/reaction/336196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chlorideHCID 21694907—

Reaction Conditions

Temperature0 °C

Reaction Steps

Thiomorpholine 1,1-dioxide (3 g; 22.192 mmol) is dissolved in THF (70 mL) and cooled to 0° C. Triethylamine (3.708 mL; 26.6 mmol) is added, followed by 20% phosgene in toluene (35.229 mL; 66.6 mmol). The reaction mixture is stirred at room temperature for 18 hours. After this time, the reaction mixture is poured into ethyl ether (200 mL), then filtered through Celite®. The Celite® is washed with ethyl ether several times and the combined filtrates are concentrated in vacuo to afford the title compound as a white solid. 1H NMR (400 MHz, d-CDCl3): δ 3.1-3.2 (m; 4H), 4.1-4.3 (d, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889670B2
Source datasetuspto-grants-2014_11
ORD IDord-81e05e5b901440919e41e58d6d38edd8
Source noteuspto-grants-2014_11