참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | 3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl- | HCID 98497 | — |
| 반응물 | chromium (VI) trioxide | HCID 10219390 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | Jones' reagent | HCID 131709961 | — |
반응 단계
A solution was made of α-campholenic aldehyde (200 g) in acetone (2 liters) and cooled to 0° C. Jones reagent was prepared from 115 ml conc. sulfuric acid, 500 ml water and 134 g of chromium (VI) oxide. The reagent (400 ml) was added to the solution at 0° C. over a period of 30 minutes. After an additional 15 minutes at 0° C. the acetone was removed by decantation and the residual chromium salts were washed with an additional 200 ml acetone. The combined acetone solution was concentrated to 1 liter, diluted with 10% aqueous sodium hydroxide (1 liter) and washed with CH2Cl2 (2×1 liter). The aqueous phase was acidified with 25% sulfuric acid and extracted with CH2Cl2 (2×1 liter). Concentration of the CH2Cl2 solution yielded an oil (145 g) which was distilled under reduced pressure to give 116 g of a yellowish liquid; bp 121° C. @ 2.2 mm Hg; analysis: 98% (CW 20M fused silica column, 180° C.) α-campholenic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04590953 |
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| 출처 데이터셋 | uspto-grants-1986_05 |
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| ORD ID | ord-bcd8fd69854f412198a9c6d8b0fb2e72 |
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| 출처 메모 | uspto-grants-1986_05 |
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