참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | cis-1,3-Cyclohexanedicarboxylic anhydride | HCID 11367118 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | cis-1,3-Cyclohexanedicarboxylic acid diethyl ester | HCID 10977233 | — |
반응 단계
Anhydride 1 (7.71 g; 50 mmol) was combined with triethyl orthoformate (12.5 mL; 75 mmol; 1.5 equiv) and ethanol (50 mL). p-Toluenesulfonic acid (0.48 g; 2.5 mmol; 0.05 equiv) was added and the reaction mixture was heated overnight at 60° C. to completely consume 1. Solid sodium bicarbonate (0.5 g) was added and the solvent was removed at reduced pressure. The residue was dissolved in toluene (25 mL), washed with saturated aqueous NaHCO3 (5 mL), dried over Na2SO4, and concentrated to afford 11.42 g (99%) of cis-2b which was a single peak by GC analysis.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06210956B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-103a8571befd42b9b33d9e2537247ea4 |
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| 출처 메모 | uspto-grants-2001_04 |
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