HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 21842580, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamide | HCID 21842621 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 21842580 | HCID 21842580 | 97% |
Reaction Steps
Methanesulfonyl chloride (0.028 mL, 41 mg, 0.36 mmol) was added dropwise over 5 min to a 0° C. solution of N-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamide (100 mg, 0.357 mmol) and triethylamine (0.075 mL, 54 mg, 0.054 mmol) in 1.0 mL of ethyl acetate. After 15 min., the resulting suspension was poured into 40 mL of ice cold ethyl acetate and washed succesively with 20 mL of ice water, 20 mL of ice cold 2.0 N HCl, 20 mL of ice water and 20 mL of brine. The ethyl acetate layer was dried over sodium sulfate and evaporated to give 128 mg of crude N-(2-methanesulfonyloxy-2-phenylethyl)-N-methylbenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962462 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-747cec38ba114688b22ecc95210adc5f |
| Source note | uspto-grants-1999_10 |