HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2R)-2-(Acetyloxy)propanoyl chloride → (r)-Acetic acid 1-[(7-benzenesulfonyl-chroman-2-ylmethyl)-carbamoyl]-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2R)-2-(Acetyloxy)propanoyl chloride | HCID 15557611 | — |
| Reactant | (R)-C-(7-Benzenesulfonyl-chroman-2-yl)-methylamine | HCID 58869146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (r)-Acetic acid 1-[(7-benzenesulfonyl-chroman-2-ylmethyl)-carbamoyl]-ethyl ester | HCID 131728243 | — |
Reaction Steps
(R)—C-(7-Benzenesulfonyl-chroman-2-yl)-methylamine (57 mg, 0.19 mmol) triethylamine (0.02 mL) and acetic acid 1-(R)-chlorocarbonyl-ethyl ester were added to 1 mL methylene chloride, and the mixture was stirred for two hours at room temperature. The reaction was quenched by addition of water, and the mixture was extracted with methylene chloride. The combined organic layers were washed with water and brine, dried (Na2SO4), filtered and contrated under reduced pressure. Purification of the residue by flash chromatography gave 7.59 mg of (R)-acetic acid 1-[(7-benzenesulfonyl-chroman-2-ylmethyl)-carbamoyl]-ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754759B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-72aea6534f9f4bbfb0aeac34df25a8fa |
| Source note | uspto-grants-2010_07 |