HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851024Generated: October 29, 2026
Acetyl chloride → HCID 12788523, compound
https://huagongshe.com/reaction/851024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12788411 | HCID 12788411 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12788523 | HCID 12788523 | — |
Reaction Steps
A solution of 1.4 ml of acetyl chloride in 75 ml of chloroform is added dropwise under nitrogen over a 15-minute period to a solution of 5.05 g of the free base of cis-4-(4-aminophenoxy)-1-methyl-3-phenylpiperidine of Example 8 in 150 ml of dry chloroform containing 2.74 ml of triethylamine. The pot temperature reaches a maximum of 28° C. The reaction is complete in 30 minutes. The chloroform solution is washed with 10% aqueous NaOH solution, then with saturated aqueous NaCl solution, dried over anhydrous Na2SO4 and concentrated in vacuo to a foam which solidifies upon trituration with hexane. The hexane mixture is briefly heated to boiling, then cooled to room temperature and allowed to stand for 30 minutes before filtering. A crude solid results, mp s 172°, 173°-175° C. Recrystallization from toluene affords cis-4-(4-acetamidophenoxy)-1-methyl-3-phenylpiperidine, mp 174.5°-176.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382141 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-1512964ba08242009fdfef1451c31f4b |
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| Source note | uspto-grants-1983_05 |
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