HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003276Generated: October 30, 2026
Trifluoroacetic acid → HCID 53767324, compound
https://huagongshe.com/reaction/1003276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 21967812 | HCID 21967812 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53767324 | HCID 53767324 | 90.5% |
Reaction Steps
(S)-4-[2-(tert-Butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yloxy]-N,N-dimethylbutyramide (396 mg) was dissolved in dichloromethane (5 ml), a solution of trifluoroacetic acid (5 ml) in dichloromethane (5 ml) was added to the solution under ice-cooling with stirring, and the mixture was still stirred for 15 minutes. After reaction at room temperature for 15 minutes, the reaction mixture was concentrated in vacuo. Dichloromethane, water and sodium bicarbonate were added to the resulting residue and the mixture was stirred at room temperature for 30 minutes. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give (S)-4-(2-amino-1,2,3,4-tetrahydronaphthalen-7-yloxy)-N,N-dimethylbutyramide (263 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046192 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-93291aade2a04a44aa76961a5f9efb91 |
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| Source note | uspto-grants-2000_04 |
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