HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 2-methanesulfonyl-3-phenylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 2-hydroxy-3-phenylbenzoate | HCID 241577 | — |
| Product | Methyl 2-methanesulfonyl-3-phenylbenzoate | HCID 22768433 | — |
Reaction Steps
An ethereal solution (1 liter) containing 50.0 g (0.22 mol) of methyl 2-hydroxy-3-phenylbenzoate, 0.25 mole of methanesulfonyl chloride and 0.25 mole of Et3N was allowed to react at room temperature for 18 hours. The reaction mixture was washed with 1 N NaOH (1 × 1 liter) and H2O (1 × 500 ml). After drying with MgSO4 the ether solution was evaporated to give a yellow solid; yield 61.9 g (91.7%), mp. 101°-115°. Recrystallization of the crude product from benzene-hexane gave the analytical sample, mp. 120°-124°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04116961 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-96c52519c78046a097b6ecad7ca34539 |
| Source note | uspto-grants-1978_09 |