HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845435Generated: October 27, 2026
Glutaric anhydride → 4-(5H-dibenzo[a,d]cyclohepten-5-yl)-delta-oxo-1-piperidinepentanoic acid
https://huagongshe.com/reaction/845435
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glutaric anhydride | HCID 7940 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(5H-Dibenzo[a,d][7]annulen-5-yl)piperidine | HCID 13753410 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(5H-dibenzo[a,d]cyclohepten-5-yl)-delta-oxo-1-piperidinepentanoic acid | HCID 14253328 | — |
Reaction Steps
0.04 gram (0.36 millimole) of 4-dimethylaminopyridine, 0.94 gram (7.26 millimoles) of ethyl diisopropylamine, and 0.41 gram (3.63 millimoles) of glutaric anhydride were added successively to a solution of 1.00 gram (3.63 millimoles) of 4-(5H-dibenzo[a,d]cyclohepten-5-yl)-piperidine and the resulting mixture stirred at ambient temperature for two hours. The reaction mixture was diluted with 100 milliliters of methylene chloride and washed with aqueous hydrochloric acid and then with brine. The washed solution was dried over magnesium sulfate, the drying agent filtered and the solution evaporated in vacuo whereupon a foam was produced which when triturated with hot acetonitrile produced white crystals. The crystals were recrystallized from hot acetic acid/acetonitrile to obtain 4-(5H-dibenzo[a,d]cyclohepten-5-yl)-δ-oxo-1-piperidinepentanoic acid product, m.p. 180°-186° C. The product had elemental analyses as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04758577 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-c42dab549b5941d09eae260fb4e34fd7 |
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| Source note | uspto-grants-1988_07 |
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