HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164832Generated: October 31, 2026
Ethylene Glycol → 6,7-dihydro-5H-dibenzo[a,c]cycloheptene-4-carboxylic acid
https://huagongshe.com/reaction/2164832
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-4-carbonitrile | HCID 13281340 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,7-dihydro-5H-dibenzo[a,c]cycloheptene-4-carboxylic acid | HCID 13281341 | — |
Reaction Steps
Under a dry nitrogen atmosphere a solution of 6,7-dihydro-5H-dibenzo[a,c]cycloheptene-4-carbonitrile (2.95 grams, 0.0134 mole), potassium hydroxide (4 grams, 0.085 mole), ethylene glycol (40 ml) and water (3 ml) was heated at reflux for approximately 24 hours. The mixture was cooled, diluted with water, and the solution was washed with diethyl ether. The aqueous solution was acidified and extracted with diethyl ether. The extract was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated to give a white solid. The solid was combined with similar material prepared in a separate experiment, and the combined solids were recrystallized from n-hexane to give 6,7-dihydro-5H-dibenzo[a,c]cycloheptene-4-carboxylic acid (mp 137°-139°) as nearly white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507317 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-722837a1aad9402d8b9878980dcd432e |
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| Source note | uspto-grants-1985_03 |
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