참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chloroacetyl chloride | HCID 6577 | — |
| 반응물 | Allylamine | HCID 7853 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,4,4-Trimethylcyclopentanone | HCID 107324 | — |
| 반응물 | 2,2,4-Trimethylcyclopentanone | HCID 119632 | — |
| 반응물 | Ammonium Sulfate | HCID 6097028 | — |
| 반응물 | N-(3,3,5-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamide | HCID 13021160 | — |
| 반응물 | N-(3,5,5-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamide | HCID 13021161 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | N-(2,4,4-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamide | HCID 13021162 | — |
반응 단계
By the same procedure as in Example 63 using a mixture comprising 2,2,4-trimethylcyclopentanone and 2,4,4-trimethylcyclopentanone (about 1:1) (25.2 parts by weight; 0.2 mole) in 0.2 liter of benzene, 0.1 part by weight of ammonium sulfate, and 11.4 parts by weight (0.2 mole) of allylamine, further reacted with 22.6 parts by weight (0.2 mole) of chloracetyl chloride in 0.05 liter of benzene and 22 parts by weight (0.2 mole) of triethylamine in 0.1 liter of benzene, a mixture of isomers consisting of N-(3,3,5-trimethylcyclopenten-1-yl)-N-allyl-α-chloroacetamide, N-(3,5,5-trimethylcyclopenten-1-yl)-N-allyl-α-chloroacetamide, and N-(2,4,4-trimethylcyclopenten-1-yl)-N-allyl-α-chloroacetamide was obtained. The yield of brown oily distillate (B.P.=88°-93° C. at 1.0 torr) having a refractive index (nD20 =1.4978) was 29 parts by weight. The content of organically combined chlorine was 15.9% (14.7%). The nitrogen content was 6.1% (5.8%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04319918 |
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| 출처 데이터셋 | uspto-grants-1982_03 |
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| ORD ID | ord-dca8fee64b6548ecab7c62a651f09001 |
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| 출처 메모 | uspto-grants-1982_03 |
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