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Thionyl Chloride → HCID 86583766, 화합물

HRID 1057269
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HRID 1057269 반응식
[C:1]([O:22][CH2:23][CH2:24][CH2:25][CH3:26])(=[O:21])[C:2]1[C:3](=[CH:7][C:8](=[C:12]([CH:20]=1)[C:13]([O:15][CH2:16][CH2:17][CH2:18][CH3:19])=[O:14])[C:9]([O-:11])=[O:10])[C:4]([O-:6])=[O:5].S(Cl)([Cl:29])=O>CN1C(=O)CCC1>[Cl-:29].[Cl-:29].[C:13]([O:15][CH2:16][CH2:17][CH2:18][CH3:19])(=[O:14])[C:12]1[C:8](=[CH:7][C:3](=[C:2]([CH:20]=1)[C:1]([O:22][CH2:23][CH2:24][CH2:25][CH3:26])=[O:21])[C:4]([O-:6])=[O:5])[C:9]([O-:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 86181797HCID 86181797, 화합물

생성물 1

HCID 86583766HCID 86583766, 화합물

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매2회

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온도
0 °C

실험 절차

Next, the NMP solution (θ) of di-n-butyl pyromellitate was added to the NMP solution (η) of di-n-butyl 3,3′,4,4′-diphenylether-tetracarboxylate, and the flask containing them was cooled to 0° C., to which was dropwise added 20.56 g (0.173 mols) of thionyl chloride, and reacted therewith for 1 hour to obtain a mixed solution (ι) of di-n-butyl 3,3′,4,4′-diphenylether-tetracarboxylate dichloride and di-n-butyl pyromellitate dichloride.

후처리

  1. additionthe flask containing them
  2. customreacted

출처 및 근거

ORD 기록
ord-131d13647bda44cbbc3f4b2b3cd6dfec
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06514658B2

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