참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | 1,1-Dimethylethyl trimethylsilylacetate | HCID 99527 | — |
| 반응물 | 2-Methylthio-6-n-hexylbenzaldehyde | HCID 15008155 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Tert-butyl 2-methylthio-6-n-hexylcinnamate | HCID 54465638 | — |
반응 단계
To a solution of lithium diisopropylamide, afforded by combining 3.4 g of diisopropylamine with 26 ml of n-butyllithium, at -40° C. in THF is added tert-butyl trimethylsilylacetate (8 g, 0.042 mmol) and the mixture stirred for 1 hour. To the reaction mixture is added 2-methylthio-6-n-hexylbenzaldehyde (7.08 g, 0.03 mmol) dropwise and stirred for 2 hours at -40° C. The reaction mixture is allowed to warm to -10° C. and cold lN HCl poured in. The mixture is extracted with diethyl ether. The extracts are washed with water and then brine, dried over MgSO4 and concentrated to afford tert-butyl 2-methylthio-6-n-hexylcinnamate which is hydrolyzed in methylene chloride with trifluoroacetic acid by refluxing overnight to afford the subtitle compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05028629 |
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| 출처 데이터셋 | uspto-grants-1991_07 |
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| ORD ID | ord-819f0ae255ac49a6a097e30ab4ddc585 |
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| 출처 메모 | uspto-grants-1991_07 |
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