HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534678Generated: October 25, 2026
Trifluoroacetic acid → N-benzyl-O-benzyl-D-serinamide
https://huagongshe.com/reaction/534678
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-benzyl-O-benzyl-N2-Boc-D-serinamide | HCID 7216909 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-benzyl-O-benzyl-D-serinamide | HCID 67082833 | 70% |
Reaction Steps
To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (3 g) and dichloromethane (15 mL), trifluoroacetic acid (15 mL) was added. The solution was stirred for 2 hours at 40° C. for completion of reaction. The solution was concentrated under vacuum to remove solvents and subsequently water was added. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layer was washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 1.55 g of N-benzyl-O-benzyl-D-serinamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853439B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-637b96a137da4747ae3a5d48b80551ca |
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| Source note | uspto-grants-2014_10 |
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