참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Isobutylene | HCID 8255 | — |
| 반응물 | Citronellic acid | HCID 10402 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Tert-butyl 3(rs),7-dimethyl-6-octenoate | HCID 22619086 | — |
반응 단계
25 ml of isobutylene were condensed at −78° C. and added to a mixture of 19.4 g (114 mmol) of 3(RS),7-dimethyl-6-octenoic acid and 1 ml of concentrated sulphuric acid in 25 ml of dichloromethane. The mixture was stirred for 24 hours under a dry ice condenser. A further 20 ml of isobutylene were added and the mixture was stirred for 24 hours under a dry ice condenser. The mixture was diluted with dichloromethane, washed with saturated sodium bicarbonate solution, dried over anhydrous magnesium sulphate and evaporated under a vacuum. The resulting oil was purified by chromatography on silica gel using ethyl acetate/hexane (1:9) for the elution. There were obtained 20.8 g of tert-butyl 3(RS),7-dimethyl-6-octenoate as a colourless oil. 1H NMR (250 MHz, CDCl3)δ: 0.9 (d, 3H), 1.1-1.3 (m,3H), 1.4 (s, 9H), 1.6 (s, 3H), 1.65, (s, 3H), 1.8-2.2 (br m, 4H), 5.05, (m, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06372883B1 |
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| 출처 데이터셋 | uspto-grants-2002_04 |
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| ORD ID | ord-bbd28a3ce2a443baaf3645c6929542dc |
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| 출처 메모 | uspto-grants-2002_04 |
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