HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196283Generated: October 26, 2026
Triethylamine → (3aR, 7aR)-2-[(RS)-2-(2-dimethylaminophenyl)propionyl]-7,7-diphenylperhydro-4-isoindolone
https://huagongshe.com/reaction/1196283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3aR,7aR)-7,7-diphenyl-4-perhydroisoindolone hydrochloride | HCID 22843247 | — |
| Reactant | 2-[2-(Dimethylamino)phenyl]propanoic acid | HCID 54100613 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3aR, 7aR)-2-[(RS)-2-(2-dimethylaminophenyl)propionyl]-7,7-diphenylperhydro-4-isoindolone | HCID 22843227 | 58% |
Reaction Steps
N,N'-carbonyldiimidazole (0.85 g) is added to a solution, cooled to 5° C., of (RS)-2-(2-dimethylaminophenyl)propionic acid (1 g) in dichloromethane (30 cc), and the mixture is stirred for 30 minutes at this temperature. A solution of (3aR, 7aR)-7,7-diphenylperhydro-4-isoindolone hydrochloride (1.7 g) and triethylamine (1.4 cc) in dichloromethane (30 cc) is added. The reaction mixture is stirred at 20° C. for 16 hours, washed with water (2×100 cc), dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (0.2-0.063 mm, diameter 3 cm, height 50 cm), eluting under a nitrogen pressure of 0.5 bar with ethyl acetate and collecting 125-cc fractions. Fractions 4 to 6 are combined and concentrated to dryness under reduced pressure (2.7 kPa) to give (3aR, 7aR)-2-[(RS)-2-(2-dimethylaminophenyl)propionyl]-7,7-diphenylperhydro-4-isoindolone (1.4 g) in the form of white meringue-like product;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112988 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-b910036bec7845c995a6e390a0a43b5a |
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| Source note | uspto-grants-1992_05 |
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