HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213026Generated: November 1, 2026
Trifluoroacetic acid → S-Acetylthioglycolic acid NHS ester
https://huagongshe.com/reaction/2213026
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 69557602 | HCID 69557602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S-Acetylthioglycolic acid NHS ester | HCID 21955272 | 67.9% |
Reaction Steps
Trifluoroacetic acid (20 mL) was added to a solution of 1-(1,1-dimethylethyl) 4-(hydroxymethyl)-4-(2-methyl-2-propenyl)-1-piperidinecarboxylate (Description 90, 1.14 g, 4.2 mmol) in dichloromethane (4 mL) and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure and water (40 mL) was added. The pH was adjusted to 12 with aqueous sodium hydroxide (4M) and the mixture was extracted with ethyl acetate (4×40 mL). The combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was dissolved in ethanol (10 mL) and ethereal hydrogen chloride (1M, 10 mL) was added. The solvent was evaporated under reduced pressure and the residue was triturated with ethyl acetate (15 mL). The solid was collected and dried in vacuo to give the title compound as a colorless solid (483 mg, 56%). m/z (ES+) 170 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07105507B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-e8e351e382bf46c6b1d7893c47242834 |
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| Source note | uspto-grants-2006_09 |
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