HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903418Generated: October 25, 2026
Glycine ethyl ester → Ethyl 4-(8-cyclohexyloctylamino)hippurate
https://huagongshe.com/reaction/903418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycine ethyl ester | HCID 12176 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | p-(8-Cyclohexyloctyl)aminobenzoyl chloride hydrochloride | HCID 20475769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 4-(8-cyclohexyloctylamino)hippurate | HCID 20475823 | — |
Reaction Steps
A solution of 18.0 g. of 4-(8-cyclohexyloctylamino)benzoyl chloride hydrochloride in 100 ml. of dioxane is added to freshly prepared ethyl glycinate in 300 ml. of CH2Cl2 containing 1 g. of dimethylaminopyridine and 10 ml. of triethylamine. After 16 hours at room temperature the reaction mixture was refluxed for 2 hours, cooled and filtered. The mother liquor is extracted with water and 10% hydrochloric acid. The solution is dried over magnesium sulfate and concentrated in vacuo to an amber liquid. A 6 g. sample is pre-absorbed on 30 g. of silica III and placed on 250 ml. of alumina and eluted with ether giving 4.2 g. of solid. Thin-layer chromatography (hexane:ethylacetate, 3:1) indicates three components so this material (3 g.) is chromatographed on silica giving a solid which is recrystallized from acetonitrile to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04227014 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-e049fe5607424230b187cbb529de57e1 |
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| Source note | uspto-grants-1980_10 |
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