HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methanesulfonyloxy-acetic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzyl 2-hydroxyacetate | HCID 561337 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methanesulfonyloxy-acetic acid benzyl ester | HCID 15742138 | 73% |
Reaction Steps
To a solution of benzyl glycolate (2.0 mL, 14.1 mmol) and triethylamine (2.35 mL, 16.9 mmol) in dichloromethane (30 mL) at 0° C. was added dropwise methanesulfonyl chloride (1.20 mL, 15.1 mL). The reaction was stirred overnight, diluted with dichloromethane, washed with saturated aqueous NH4Cl, and then with saturated NaHCO3, dried with Na2SO4, and concentrated in vacuo to give 2.50 g (73%) of methanesulfonyloxy-acetic acid benzyl ester which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776855B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-9939d3b733c347c388b142a882c23ed1 |
| Source note | uspto-grants-2010_08 |