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Acrylic Acid → Ethylacrylate acrylic acid acrylonitrile

HRID 1194281
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HRID 1194281 반응식
[C:1]([O:5][CH2:6][CH3:7])(=[O:4])[CH:2]=[CH2:3].[C:8](#[N:11])[CH:9]=[CH2:10].[C:12]([OH:16])(=[O:15])[CH:13]=[CH2:14].C(S)CCCCCCCCCCC.C(OOCCCCCCCCCCCC)CCCCCCCCCCC.C(OOC(=O)C1C=CC=CC=1)CCC>C1(C)C(C)=CC=CC=1>[CH2:6]([O:5][C:1](=[O:4])[CH:2]=[CH2:3])[CH3:7].[C:12]([OH:16])(=[O:15])[CH:13]=[CH2:14].[C:8](#[N:11])[CH:9]=[CH2:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 6581Acrylic AcidHCID 7855AcrylonitrileHCID 81951-DodecanethiolHCID 8821Ethyl AcrylateHCID 76169Lauryl peroxideHCID 83282Butyl perbenzoate

생성물 1

HCID 168852Ethylacrylate acrylic acid acrylonitrile

시약·촉매·용매 1

HCID 7237O-Xylene용매2회

실험 절차

this polymer material was produced by adding to 320g xylene at 100° C. the monomer solution and a catalyst solution over a period of 3 hours. The monomer solution contained 2.900g ethyl acrylate, 76g acrylonitrile, 76g acrylic acid and 3g laurylmercaptan. The catalyst solution contained 26g laurylperoxide and 7g butylperbenzoate in 273g of xylene. The material was highly viscous with comonomer proportions of 95:2.5:2.5.

후처리

  1. customthis polymer material was produced

출처 및 근거

ORD 기록
ord-b49eff8d34704bb290fcc0074a7ddde4
출처 데이터셋
uspto-grants-1989_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04814215

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