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Nitrogen → HCID 14010414, 화합물

HRID 2292183
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HRID 2292183 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]=[N:9][C:10]2[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=2)=[CH:4][CH:3]=1.[C:17](Cl)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19].N#N.[OH2:26]>N1C=CC=CC=1>[C:17]([O:16][C:13]1[CH:14]=[CH:15][C:10]([N:9]=[N:8][C:5]2[CH:4]=[CH:3][C:2]([O:1][C:17](=[O:26])[C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:7][CH:6]=2)=[CH:11][CH:12]=1)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 947NitrogenHCID 962WaterHCID 62493Pivaloyl chlorideHCID 1012454,4'-Dihydroxyazobenzene

생성물 1

HCID 14010414HCID 14010414, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

1 g (0.0047 mole) of 4,4'-dihydroxyazobenzene and 2 g (0.016 mole) of pivaloyl chloride was stirred in 20 mls of pyridine for 24 hrs. at room temperature. The solvent was blown off under a stream of N2. Water was added and the crude product filtered and recrystallized from ethanol; 1.5 g (83%) yield. M.P.~185°-188° C.

후처리

  1. customat room temperature
  2. filtrationthe crude product filtered
  3. customrecrystallized from ethanol
  4. custom1.5 g (83%) yield

출처 및 근거

ORD 기록
ord-a2f41aac224e448c85ceae68b154332e
출처 데이터셋
uspto-grants-1989_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04801610

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