HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439173Generated: November 1, 2026
2-Benzoylbenzoic Acid → HCID 21398396, compound
https://huagongshe.com/reaction/1439173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Benzoylbenzoic Acid | HCID 6813 | — |
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | N-Propylpropane-1,3-diamine | HCID 90250 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21398396 | HCID 21398396 | — |
Reaction Steps
22.6 Parts of o-benzoyl-benzoic acid and 11.6 parts of N-propyl-1,3-propanediamine are haeted within 11/2 hours with 50 parts by volume of o-dichlorobenzene until the boiling point of the latter is attained. Almost the theoretical amount of reaction water is azeotropically distilled off. The clear solution is evaporated to dryness in vacuo, the oily residue is dissolved in ethyl acetate and crystallised by the dropwise addition of pentane. In this way, 1-propyl-10b-phenyl-1,3,4,10b-tetrahydro-pyrimido[2,1-a]isoindol-6(2H)-one is obtained of the formula ##STR19## M.P. 135°-137°. 1-Ethyl-10b-phenyl-1,3,4,10b-tetrahydro-pyrimido[2,1-a]isoindol -6(2H)-one is obtained in the same manner from o-benzoyl-benzoic acid and N-ethyl-1,3-propanediamine. M.P. 131°-133°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04058529 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-9ec9e32eb84549c7a900d2c8f12a4ce5 |
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| Source note | uspto-grants-1977_11 |
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