HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389939Generated: October 30, 2026
HCID 20296014, compound → HCID 20295984, compound
https://huagongshe.com/reaction/1389939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20296014 | HCID 20296014 | — |
| Reactant | Potassium hydroxide ethanol | HCID 21946426 | — |
| Product | HCID 20295984 | HCID 20295984 | — |
Reaction Steps
A mixture of 12.7 parts of 2-(2,6-dichlorophenyl)-2-(2-naphthylamino) acetamide and 250 parts of potassium hydroxide/ethanol 1 N is stirred and refluxed for 48 hours. The reaction mixture is evaporated. The oily residue is dissolved in 400 parts of water and the solution is acidified with concentrated hydrochloric acid solution. The sticky product is extracted with 1,1'-oxybisethane. The extract is washed twice with water, dried and evaporated. The oily residue is triturated three times in petroleumether. The solid product is filtered off and recrystallized from 50 parts of glacial acetic acid. The product is washed with petroleumether, dried and dissolved in 80 parts of 1,1'-oxybisethane. The solution is stirred with activated charcoal, filtered and the filtrate is evaporated. The oily residue solidifies on triturating in 2-propanol and petroleumether. The solid is filtered off and dried, yielding 1.6 parts of 2-(2,6-dichlorophenyl)-N-(2-naphthyl)glycine; mp. 171.7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04246429 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-ac3fda0daa6744ef8cacb3ee5f3b7b1b |
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| Source note | uspto-grants-1981_01 |
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