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HCID 14365936, 화합물 → 2,5-Diamino-1,4-benzenedithiol

HRID 1762966
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HRID 1762966 반응식
Cl.Cl.[NH2:3][C:4]1[CH:9]=[C:8]([SH:10])[C:7]([NH2:11])=[CH:6][C:5]=1[SH:12].O1C2C=CC=CC=2N=C1C1C(C(O)=O)=CC=C(C(O)=O)C=1>>[NH2:3][C:4]1[CH:9]=[C:8]([SH:10])[C:7]([NH2:11])=[CH:6][C:5]=1[SH:12]
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참가 물질

3

반응물 2

HCID 14365936HCID 14365936, 화합물HCID 146182692,5-Diaminobenzene-1,4-dithiol--hydrogen chloride (1/2)

생성물 1

HCID 45983552,5-Diamino-1,4-benzenedithiol

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온도
90 °C

실험 절차

2,5-Diamino-1,4-benzene dithiol dihydrochloride (1.5544 g, 6.3 mmol), 2-benzoxazole terephthalic acid (1.7956 g, 6.3 mmol) and 10.2 g of polyphosphoric acid (83% P2O5) were placed in a resin flask equipped with a mechanical stirrer, nitrogen inlet/outlet tubes, a vacuum connector and a side opening on the resin flask. With nitrogen continuously flowing, the solution was heated slowly to 60° C. for 24 hours and 90° C. for 16 hours to remove the hydrochloride. The mixture was heated at 160° C. for 17 hours, then at 190° C. for 17 hours. Work-up, as in the preceeding Example, gave a polymer with [N]=0.96 dl/g, methanesulfonic acid at 30° C.

후처리

  1. customequipped with a mechanical stirrer, nitrogen inlet/outlet tubes
  2. customto remove the hydrochloride
  3. temperatureThe mixture was heated at 160° C. for 17 hours
  4. customat 30° C.

출처 및 근거

ORD 기록
ord-73291f375575464d818581778afa6886
출처 데이터셋
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04835246

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