HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322694Generated: October 29, 2026
Trifluoroacetic acid → HCID 86585123, compound
https://huagongshe.com/reaction/322694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 69623028 | HCID 69623028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86585123 | HCID 86585123 | — |
Reaction Steps
(S)-2-(tert-Butoxycarbonylamino)-2-(6-methoxy-2-naphthyl)acetic acid was then converted into the methyl ester using General Procedure G below. The methyl ester was then dissolved in CH2Cl2 and this solution cooled to 0° C. Trifluoroacetic acid (50 molar eq.) was added and the reaction was allowed to warm to room temperature and stirring was continued for 2 hrs. The reaction mixture was then concentrated and the residue extracted into CH2Cl2 and washed with sodium bicarbonate solution. The organic layer was dried over Na2SO4, filtered and concentrated to yield methyl (S)-2-amino-2-(6-methoxy-2-naphthyl)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211235B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-254051ecf4eb4c31ac9245303e4e2a86 |
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| Source note | uspto-grants-2001_04 |
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