참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Dibenzosuberone | HCID 14589 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | HCID 178418630 | HCID 178418630 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Cyclopropyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ol | HCID 19261382 | — |
반응 단계
A solution of cyclopropylmagnesium bromide in dry THF (prepared from cyclopropylbromide (12.1 g, 0.10 mol), magnesium turnings (2.45 g, 0.10 mol) and dry THF (65 ml)) was placed under an atmosphere of nitrogen. A solution of 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one (10.4 g, 0.05 mol) in dry THF (25 ml) was added dropwise and when addition was complete the mixture was heated at reflux for 30 minutes. The reaction mixture was cooled on an ice-bath and saturated ammonium chloride (50 ml) was carefully added. The mixture was neutralized with 2N hydrochloric acid and extracted with diethyl ether (2×200 ml). The combined organic extracts were dried (Na2SO4) and the solvent was evaporated in vacuo to give 13.1 g of crude 5-cyclopropyl-10,11 -dihydro-5H-dibenzo[a,d]cyclohepten-5-ol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05712292 |
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| 출처 데이터셋 | uspto-grants-1998_01 |
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| ORD ID | ord-1b61f63768324f12abc7e252fae57998 |
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| 출처 메모 | uspto-grants-1998_01 |
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