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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2058940생성일: 2026년 10월 26일

Chloroacetyl chloride → N-(2,4,4-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamide

https://huagongshe.com/reaction/2058940

반응식

참여 물질

역할이름HCID투입량
반응물Chloroacetyl chlorideHCID 6577—
반응물AllylamineHCID 7853—
반응물TriethylamineHCID 8471—
반응물2,4,4-TrimethylcyclopentanoneHCID 107324—
반응물2,2,4-TrimethylcyclopentanoneHCID 119632—
반응물Ammonium SulfateHCID 6097028—
반응물N-(3,3,5-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamideHCID 13021160—
반응물N-(3,5,5-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamideHCID 13021161—
용매BenzeneHCID 241—
생성물N-(2,4,4-trimethylcyclopenten-1-yl)-N-allyl-alpha-chloroacetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04319918
출처 데이터셋uspto-grants-1982_03
ORD IDord-dca8fee64b6548ecab7c62a651f09001
출처 메모uspto-grants-1982_03