참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | (2-Carboxyethyl)triphenylphosphonium chloride | HCID 10270534 | — |
| 반응물 | 9,10-Methanoanthracene-9(10H)-carbaldehyde | HCID 12404141 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | gamma-(9,10-Dihydro-9,10-methano-9-anthryl)-beta-butenoic acid | HCID 54474651 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04224344 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-6a1bcab99e7646dca3cfbb7012c89a4b |
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| 출처 메모 | uspto-grants-1980_09 |
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