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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiomorpholine 1,1-dioxide | HCID 6484228 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1-Dioxo-1lambda6-thiomorpholine-4-carbonyl chloride | HCID 21694907 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08889670B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-81e05e5b901440919e41e58d6d38edd8 |
|---|
| Source note | uspto-grants-2014_11 |
|---|