HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089154Generated: October 30, 2026
4-Phenylbutyric Acid → HCID 15704414, compound
https://huagongshe.com/reaction/1089154
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenylbutyric Acid | HCID 4775 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15704414 | HCID 15704414 | 83.7% |
Reaction Steps
4-Phenylbutyric acid (2.46 g, 15 mmol) was dissolved in distilled tetrahydrofuran (70 ml) in an argon atmosphere. After cooling in an ice bath, carbonyl diimidazole (2.43 g, 15 mmol) was added and the mixture was stirred cold 1 hour and at room temperature 1 hour. The mixture was then cooled and glycine ethyl ester.hydrochloride (2.09 g, 15 mmol) and distilled triethylamine (2.1 ml, 15 mmol) were added. The mixture was left stirring overnight at room temperature. After removal of the solvent in vacuo, ethyl ether (200 ml) was added. The solution was washed with 1 N hydrochloric acid (70 ml), 0.5 N sodium hydroxide (70 ml) and saturated sodium chloride solution (70 ml), dried over anhydrous magnesium sulfate and freed of solvent in vacuo leaving the title I compound (3.13 g) as white crystalline material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04965279 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-c7af2218c6ac44b49966b5d696dbe8b2 |
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| Source note | uspto-grants-1990_10 |
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