HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928118Generated: November 1, 2026
Trifluoroacetic acid → HCID 178510572, compound
https://huagongshe.com/reaction/928118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178472362 | HCID 178472362 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178510572 | HCID 178510572 | — |
Reaction Steps
The crude mixture from Step 1 was dissolved in methanol (3 mL), and sodium hydroxide (1.0 M in water, 0.950 mL, 0.950 mmol) was added to the resulting solution. The reaction mixture was then heated to a temperature of 50° C. for 30 minutes. The reaction was subsequently cooled, acidified with TFA (0.1 mL) and concentrated to afford racemic trans-4-[amino(5-bromo-1,3-thiazol-2-yl)methyl]cyclohexanecarboxylic acid, which was used in subsequent synthetic transformations without purification. MS ESI calc'd. for C11H15BrN2O2S [M+H]+ 319, 321. found 319, 321.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290490B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-de07c11461d24bd88bfb58d9db13e6f4 |
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| Source note | uspto-grants-2016_03 |
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