HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide → (R)-N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide | HCID 58869170 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamide | HCID 16225763 | 23,518.9% |
Reaction Steps
(R)—N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide (100 mg, 0.22 mmol) and Perlman's catalyst (12 mg) were added to 15 mL MeOH and hydrogenated for 18 hours at 1.5 atmospheres of hydrogen. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography to give 18.7 g of (R)—N-(7-Benzenesulfonyl-chroman-2-ylmethyl)-2-hydroxy-acetamide, MS (M+H)=362.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754759B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-f305fc8ed78346a9aef351fe875f5d3f |
| Source note | uspto-grants-2010_07 |