HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703516Generated: October 30, 2026
4-Phenylbutyric Acid → HCID 18642608, compound
https://huagongshe.com/reaction/703516
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Phenylbutyric Acid | HCID 4775 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Benzyl octahydrocyclopenta[b]pyrrole-2-carboxylate--hydrogen chloride (1/1) | HCID 13216857 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18642608 | HCID 18642608 | 88% |
Reaction Steps
4.92 g (30 mmol) of 4-phenylbutyric acid are dissolved together with 8.4 ml of triethylamine in 200 ml of dry tetrahydrofuran. While cooling in ice, 2.9 ml of ethyl chloroformate are added dropwise. After stirring at 0° C. for 1 hour, 7.4 g of benzyl (2S,3aS,6aS)-octahydrocyclopenta[b]pyrrole-2-carboxylate hydrochloride are added, and the mixture is stirred at room temperature for a further 12 hours. Filtration is followed by concentration, and the residue is taken up in 3% NaHCO3 /ethyl acetate. The organic phase is separated off and washed with 10% strength citric acid, 3% strength NaHCO3 solution and saturated brine, once each, dried with MgSO4 and concentrated. Chromatography on silica gel with ethyl acetate/cyclohexane (1:2) as mobile phase results in 9.05 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983623 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-b72469dace0946a3868f4b3d0e6e705c |
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| Source note | uspto-grants-1991_01 |
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