HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624278Generated: November 2, 2026
Acetyl chloride → Tert-butyl 4-(4-acetamidophenylthio)piperidine-1-carboxylate
https://huagongshe.com/reaction/624278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 4-(4-aminophenylthio)piperidine-1-carboxylate | HCID 18538812 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(4-acetamidophenylthio)piperidine-1-carboxylate | HCID 68752092 | — |
Reaction Steps
To a 10 mL round-bottomed flask was added tert-butyl 4-(4-aminophenylthio)piperidine-1-carboxylate (100 mg, 0.324 mmol) and triethylamine (249 μl, 1.783 mmol) in dichloromethane (3242 μl). The mixture was cooled to −78° C. and acetyl chloride (115 μl, 1.621 mmol) was added. The solution was warmed to room temperature, stirred for 1 h and then diluted with water and additional dichloromethane. The aqueous phase was extracted twice with dichloromethane and the combined organics were dried with sodium sulfate, filtered and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09302989B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-b2f3763f6c3244079a729d30c90f60d0 |
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| Source note | uspto-grants-2016_04 |
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