HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047372Generated: October 30, 2026
Chloroacetyl chloride → HCID 178440755, compound
https://huagongshe.com/reaction/1047372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | HCID 13078442 | HCID 13078442 | — |
| Reactant | HCID 66851791 | HCID 66851791 | — |
| Reactant | HCID 178526690 | HCID 178526690 | — |
| Product | HCID 178440755 | HCID 178440755 | 72% |
Reaction Steps
1-[4-(4-Butyl-phenyl)-piperidin-1-yl]-2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-ethanone was prepared using a two-step synthesis. In the first step, 1-chloracetyl-4-(4-butyl-phenyl)-piperidine (also known as 1-[4-(4-butyl-phenyl)-piperidin-1-yl]-2-chloroethanone) was prepared with a 72% yield from 4-(4-butyl-phenyl)-piperidine (prepared in accordance with Example 9) and chloroacetyl chloride using the procedure illustrated in Example 4. In the second step, the 1-[4-(4-butyl-phenyl)-piperidin-1-yl]-2-[trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexyloxy]-ethanone was prepared from the 1-chloracetyl-4-(4-butyl-phenyl)-piperidine and trans-4-(4-nitro-3-trifluoromethyl-phenylamino)-cyclohexanol (prepared in accordance with Example 5) using the procedure illustrated in Example 11. This afforded the product as a yellow solid (36% yield). The structure was confirmed using Protocol II-A. Calculated mass=548; observed mass=548; HPLC retention time=4.92 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569495B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-1343511856c846b49f976513b8204709 |
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| Source note | uspto-grants-2013_10 |
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