HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxyacetyl chloride → (R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxyacetyl chloride | HCID 177085 | — |
| Reactant | (R)-C-(7-Benzenesulfonyl-chroman-2-yl)-methylamine | HCID 58869146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide | HCID 58869170 | — |
Reaction Steps
(R)—C-(7-Benzenesulfonyl-chroman-2-yl)-methylamine (130 mg, 0.43 mmol) triethylamine (0.3 mL) and benzyloxy acetyl chloride 77 uL) were added to 3 mL methylene chloride at 0° C. The reaction mixture was stirred at room temperature for three hours and then quenched by addition of water. The mixture was extracted with methylene chloride and 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 4.34 mg of (R)—N-(7-benzenesulfonyl-chroman-2-ylmethyl)-2-benzyloxy-acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754759B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-c8e8d311bc2d4d5fb2525daa686d19ce |
| Source note | uspto-grants-2010_07 |