HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-benzyl-O-benzyl-D-serinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-benzyl-O-benzyl-N2-Boc-D-serinamide | HCID 7216909 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-benzyl-O-benzyl-D-serinamide | HCID 67082833 | 93% |
Reaction Steps
To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (16 g) and dichloromethane (80 mL), trifluoroacetic acid (80 mL) was added. The solution was stirred for 2 hours and the reaction was monitored for completion of reaction. The solution was concentrated under vacuum to obtain solid which was dissolved in water. The aqueous solution was basified to pH 8-10 with 5% sodium hydroxide and was extracted with ethyl acetate. The organic layer was separated and washed with a brine solution. The organic layer was concentrated under vacuum to obtain an oily residue 11 g of N-benzyl-O-benzyl-D-serinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853439B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-890a981e1f84428a901e3d86c71b343c |
| Source note | uspto-grants-2014_10 |