HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methanesulfonic acid 3-benzenesulfonyl-3-methylbutyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-Benzenesulfonyl-3-methyl-butan-1-ol | HCID 14906979 | — |
| Product | Methanesulfonic acid 3-benzenesulfonyl-3-methylbutyl ester | HCID 86595010 | 103.1% |
Reaction Steps
A solution of 3-benzenesulfonyl-3-methyl-butan-1-ol (2.17 g, 9.5 mmol), triethylamine (2.0 ml, 14.25 mmol), methanesulphonyl chloride (0.9 ml, 11.78 mmol) and 4-N,N-dimethylaminopyridine (12 mg, 0.01 mmol) was stirred at 0° C. for 45 min. After quenching with satd. NaHCO3, the mixture was extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated to give the title product (3.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101892B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-4f69f1bcb9d44b4b9564223aaaf7654c |
| Source note | uspto-grants-2006_09 |