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Ammonium Chloride → HCID 178488256, 화합물

HRID 274516
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HRID 274516 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[C:9]([N+:13]([O-:15])=[O:14])[C:10]=1[O:11]C)[C:6]#[N:7].[Cl-].[NH4+].[N-:18]=[N+:19]=[N-:20].[Na+]>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:6]2[NH:20][N:19]=[N:18][N:7]=2)[CH:8]=[C:9]([N+:13]([O-:15])=[O:14])[C:10]=1[OH:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium Chloride2회HCID 33557Sodium Azide2회HCID 214590491222880-77-4

생성물 1

HCID 178488256HCID 178488256, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4.0 g of 3,4-dimethoxy-5-nitro-benzonitrile are dissolved in 50 ml of dimethylformamide, whereupon the solution is treated with 1.66 g of ammonium chloride and 2.02 g of sodium azide and stirred at 125° for 31 hours. After in each case 8 and 15 hours the same amounts of ammonium chloride and sodium azide are added thereto. After cooling the mixture is poured on to ice. The separated precipitate is filtered under suction, washed with water and dried. There is obtained 2-methoxy-6-nitro-4-(1H-tetrazol-5-yl)phenol in the form of orange crystals of m.p. >240° (dec.).

후처리

  1. temperatureAfter cooling the mixture
  2. additionis poured on to ice
  3. filtrationThe separated precipitate is filtered under suction
  4. washwashed with water
  5. customdried

출처 및 근거

ORD 기록
ord-bb2e12d49b9f4b7a9b3b8c3eef73edfa
출처 데이터셋
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05389653

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