돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 554062생성일: 2026년 10월 26일

2-Chloroethanol → HCID 131729245, 화합물

https://huagongshe.com/reaction/554062

반응식

참여 물질

역할이름HCID투입량
반응물2-ChloroethanolHCID 34—
반응물Potassium CarbonateHCID 11430—
반응물Hexamethylene diisocyanateHCID 13192—
반응물2-Hydroxyethyl MethacrylateHCID 13360—
반응물CardanolHCID 11266523—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 131729245HCID 13172924562%

반응 조건

온도50 °C

반응 단계

Cardanol was modified by coupling it with 2-chloroethanol in presence of K2CO3 and KI in DMF under inert atmosphere. Hexamethylene diisocyanate [HMDI] (0.49 g, 0.003 moles) in 10 ml dry DMF was taken in a 100 ml two necked flask and the contents were cooled with ice. HEMA (0.38 g, 0.003 moles) was added drop wise with constant stirring under nitrogen. The reaction was allowed to proceed under ice cold condition for 2 hr. Then the reaction was kept at room temperature for 1 hr. After that the reaction was changed to ice cold condition and 3 drops of DBTDL was added as catalyst followed by drop wise addition of modified cardanol (1 g, 0.003 moles) in 10 ml DMF. It was left stirring under cold condition for a further 1 hr and allowed to attain room temperature. Then the reaction was heated to 50° C. for 12 hrs. The contents were poured to 150 ml water and extracted with dichloromethane. It was then washed with plenty of water and dried in vacuum oven at 60° C. for 12 hrs. Yield=62% (1.17 g). The same synthetic procedure is adopted for all types of variation in the diisocyanate chemistry or in the hydroxy(meth)acryloxy chemistry or natural resource with active hydrogen atom to obtain the final UV curable telechelic pre polymer with varying R1, R2, R3, R4, R5 and R6.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048979B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-40762ffc358245eabd6dd48c30a9c1a1
출처 메모uspto-grants-2011_11