HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86761097, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Boc-3-pyrrolidinol | HCID 4416939 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86761097 | HCID 86761097 | 191.3% |
Reaction Steps
Triethylamine (4.5 ml, 32.0 mmol) was added to a stirred solution of, N-(tert-butoxy-carbonyl)-3-hydroxypyrrolidine (2.00 g, 10.7 mmol) in diethyl ether (100 ml) and the reaction was cooled to 0° C. before addition of methanesulphonyl chloride (1.65 ml, 21.4 mmol) and stirring for 2 hours, warming from 0° C. to ambient temperature. The reaction was filtered, the filtrate was washed with 1.0 N hydrochloric acid (100 ml) and with brine (100 ml) before being dried over magnesium sulphate. Solvent evaporation in vacuo yielded N-(tert-butoxycarbonyl)-3-hydroxypyrrolidine methanesulphonate (2.9 g, 100% yield) as a colourless oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709479B1 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-d6384683522e401cadb1a8953d93b1d3 |
| Source note | uspto-grants-2010_05 |