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Hydrochloric Acid → 5-(4-Methylphenyl)-1H-tetrazole

HRID 2267966
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HRID 2267966 반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH3:9])=[CH:5][CH:4]=1)#[N:2].[N-:10]=[N+:11]=[N-:12].[Na+].[Cl-].[NH4+].Cl>O.CN(C)C=O>[CH3:9][C:6]1[CH:7]=[CH:8][C:3]([C:1]2[N:2]=[N:10][NH:11][N:12]=2)=[CH:4][CH:5]=1
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 7724p-TolunitrileHCID 25517Ammonium ChlorideHCID 33557Sodium Azide

생성물 1

HCID 2851645-(4-Methylphenyl)-1H-tetrazole수율 71.8%

시약·촉매·용매 2

HCID 962Water용매
HCID 6228
Dimethylformamide
용매

실험 절차

A stirred solution of 117 grams (1.0 mole) of 4-cyanotoluene, 65.0 grams (1.0 mole) of sodium azide, and 12.0 grams (0.224 mole) of ammonium chloride 800 mL of N,N-dimethylformamide was heated at 130° C. for three hours. After this time the reaction mixture was cooled and then poured into 800 mL of water and 400 mL of ice. The resulting mixture was acidified to pH 2 with 3N hydrochloric acid, and the resulting solid was collected by filtration. The solid was washed with hexane, triturated with 300 mL of methanol, and dried under reduced pressure to a constant weight, yielding 115 grams of 4-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole. The NMR spectrum was consistent with the proposed structure.

후처리

  1. temperatureAfter this time the reaction mixture was cooled
  2. filtrationthe resulting solid was collected by filtration
  3. washThe solid was washed with hexane
  4. customtriturated with 300 mL of methanol
  5. customdried under reduced pressure to a constant weight

출처 및 근거

ORD 기록
ord-9a1441a4b5f64430a5f8430b3bae6d68
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USH0002007H1

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