HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1523403Generated: November 2, 2026
Chloroacetyl chloride → 2-Chloro-N-[4-[(1-cyclobutyl-4-piperidinyl)oxy]phenyl]acetamide
https://huagongshe.com/reaction/1523403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23151271 | HCID 23151271 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-N-[4-[(1-cyclobutyl-4-piperidinyl)oxy]phenyl]acetamide | HCID 68287180 | 72% |
Reaction Steps
Triethylamine (66.5 g, 0.658 moles) was added to a solution of 4-[(1-Cyclobutyl-4-piperidinyl)oxy]aniline (81 g, 0.329 moles, obtained in preparation 1) in dichloromethane (1 L), at 0° C. under nitrogen atmosphere. Then the resulting mass was treated with a solution of chloro acetyl chloride (44.6 g, 0.395 moles) in dichloromethane (1 L) drop wise at 0° C. and stirred at 0° C. for 1 hour. The reaction mixture was washed with water, dried over sodium sulfate and concentrated under vacuum and the crude compound thus obtained was purified by flash chromatography (methanol:chloroform, 2:8) to obtain the title compound 76.1 g (Yield: 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079888B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-d1f7ce2248a245a6b3342539e22c8202 |
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| Source note | uspto-grants-2015_07 |
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