반응식
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][CH:4]=1)#[N:2].Cl.C(N(CC)CC)C.[N-:21]=[N+:22]=[N-:23].[Na+].O>C1(C)C=CC=CC=1>[NH:21]1[C:1]([C:3]2[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][CH:4]=2)=[N:2][N:23]=[N:22]1참가 물질
6
실험 절차
1.16 g (10 mmol) of methyl 4-cyanobenzoate, 2.06 g (15 mmol) of triethylamine hydrochloride and 0.98 g (15 mmol) of sodium azide in toluene (20 ml) was allowed to react at 100° C. for 16 hours, and after cooling to room temperature, water (20 ml) was added, and the reaction solution was allowed to separate. Concentrated hydrochloric acid was added to the aqueous layer, and the precipitated colorless solid was collected by filtration through a Kiriyama funnel and dried under reduced pressure to obtain methyl 4-(1H-tetrazol-5-yl)benzoate (1.96 g, yield 96%).
후처리
- customto react at 100° C. for 16 hours
- customto separate
- additionConcentrated hydrochloric acid was added to the aqueous layer
- filtrationthe precipitated colorless solid was collected by filtration through a Kiriyama funnel
- customdried under reduced pressure
출처 및 근거
- ORD 기록
- ord-22dbf1ff3bc84e5ea39efa4f046eef76
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08889732B2
연결된 노트
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