HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (r)-n-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-(r)-hydroxy-propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | (r)-Acetic acid 1-[(7-benzenesulfonyl-chroman-2-ylmethyl)-carbamoyl]-ethyl ester | HCID 131728243 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (r)-n-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-(r)-hydroxy-propionamide | HCID 66917474 | 542.1% |
Reaction Steps
(R)-Acetic acid 1-[(7-benzenesulfonyl-chroman-2-ylmethyl)-carbamoyl]-ethyl ester (7.59 mg) was dissolved in 1 mL MeOH, and water (0.25 mL) and LiOH (200 mg) were added. The reaction was stirred at room temperature for two hours, then quenched by addition of water. Crystals formed and were collected by filtration, washed with water and dried under vacuum to give 37 mg of (R)—N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-(R)-hydroxy-propionamide. MP=129.5-131.5° C.; MS (M−H)=374.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754759B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-1694d3fd0d034a568ca8e01a24927748 |
| Source note | uspto-grants-2010_07 |