HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethyl chloroformate → Thiomorpholine 1,1-dioxide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethyl chloroformate | HCID 12305 | — |
| Reactant | Thiomorpholine, 4-methyl-, 1,1-dioxide | HCID 91413 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Thiomorpholine 1,1-dioxide hydrochloride | HCID 12324096 | 36.1% |
Reaction Steps
2-Chloroethyl chloroformate (0.72 ml, 6.7 mmol) was added dropwise to a solution of 4-methylthiomorpholine-1,1-dioxide (11.0 g, 6.7 mmol) in toluene (10 ml) at 0° C. under N2. After 10 min, the reaction was warmed and maintained at reflux for 2 h. On cooling, the reaction mixture was evaporated, partitioned between EtOAc and H2O, the organic layer separated and washed sequentially with dilute HCl and saturated brine, the organic layer dried over Na2SO4 and evaporated. The residue was taken up in MeOH (10 ml) and heated at reflux for 2 h, after which time the reaction mixture was evaporated and triturated with EtOAc to afford the subtitle compound (415 mg, 36%) as a solid. Rf 0.34 (CH2Cl2/MeOH/0.88NH3 90/10/1, v/v). MS m/z 136 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06750214B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-209aaa7091e343ba9e3433e36dbc757c |
| Source note | uspto-grants-2004_06 |