HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27964Generated: October 25, 2026
Hydrochloric Acid → gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid
https://huagongshe.com/reaction/27964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2-Carboxyethyl)triphenylphosphonium chloride | HCID 10270534 | — |
| Reactant | 9,10-Dihydro-9,10-methanoanthracene-9-carboxaldehyde | HCID 12404141 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid | HCID 54474651 | — |
Reaction Steps
To a mixture of 9-formyl-9,10-dihydro-9,10-methanoanthracene (110 mg) and β-carboxyethyltriphenylphosphonium chloride (186 mg) in dimethylsulfoxide (2 ml) and tetrahydrofuran (2 ml) was added 65.4% sodium hydride dispersion in mineral oil (37 mg) at 0° C. under nitrogen. The reaction mixture was stirred at 0° C. for 6 hours, diluted with water, acidified with hydrochloric acid and extracted with benzene. The benzene extract was shaken with 2 N aqueous sodium hydroxide. The basic layer was acidified with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract was washed with water, dried over anhydrous sodium sulfate and evaporated to dryness to give γ-(9,10-dihydro-9,10-methano-9-anthryl)-β-butenoic acid. M.P. 166°-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04224344 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-6a1bcab99e7646dca3cfbb7012c89a4b |
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| Source note | uspto-grants-1980_09 |
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