참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Allyl chlorodifluoroacetate | HCID 10012339 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 생성물 | 2,2-Difluoro-4-pentenoic acid | HCID 11954656 | — |
반응 단계
100.0 g (0.59 mol) of allyl chlorodifluoroacetate, 42.2 g (0.65 mol) of zinc dust (activated according to Fieser & Fieser), 96.7 g (0.88 mol) of trimethylchlorosilane and 400 ml of absolute acetonitrile are introduced together into a glass autoclave, a spatula tip of iodine is added and the mixture is heated for 48 hours at 100° C. The zinc salt which has precipitated is filtered off, the filtrate is hydrolysed with H2O and rendered basic with 2N NaOH. The dark brown aqueous phase, extracted with pentane, is acidified with half-concentrated HCl, and the product is extracted with ethyl acetate. After the organic phase has been dried over MgSO4 and evaporated in a rotary evaporator (RE), the residue is distilled in vacuo. Yield: 59.4 g (74%) of a colourless oil of boiling point 73°-75° C./15.6 mbar.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04892962 |
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| 출처 데이터셋 | uspto-grants-1990_01 |
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| ORD ID | ord-3b5bd5bdad2344b08f05f11c901ccccb |
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| 출처 메모 | uspto-grants-1990_01 |
|---|