2-(Chloromethyl)aniline hydrochloride → HCID 15027412、化合物
反応式
[SH:1][C:2]1[NH:6][C:5]2[CH2:7][CH2:8][CH2:9][CH2:10][C:4]=2[N:3]=1.Cl.[NH2:12][C:13]1[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=1[CH2:15]Cl>C(O)C>[NH2:12][C:13]1[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=1[CH2:15][S:1][C:2]1[NH:6][C:5]2[CH2:7][CH2:8][CH2:9][CH2:10][C:4]=2[N:3]=1参加物
実験手順
To a suspension of 1.5 g (purity 75%, 7.3 mmol) of 2-mercapto-4,5,6,7-tetrahydro-1H-benzimidazole in 15 ml of ethanol was added 1.3 g (7.3 mmol) of 2-aminobenzyl chloride hydrochloride, and the mixture was stirred for 2 hrs. at room temperature. Ethanol was distilled off under reduced pressure at room temperature. The residue was made alkaline by addition of saturated aqueous sodium hydrogencarbonate and then extracted with 40 ml of chloroform. The chloroform portion was washed with 10 ml of 0.2N NaOH and then with saturated aqueous sodium chloride. The washed chloroform portion was dried over anhydrous sodium sulfate and placed under reduced pressure to distill off the solvent. The residue was purified by silica gel column chromatography using chloroform-methanol to give 1.35 g of the desired compound as a pale yellow oil, yield 71.4%.
後処理
- customat room temperature
- distillationEthanol was distilled off under reduced pressure at room temperature
- additionby addition of saturated aqueous sodium hydrogencarbonate
- extractionextracted with 40 ml of chloroform
- washThe chloroform portion was washed with 10 ml of 0.2N NaOH
- dry with materialThe washed chloroform portion was dried over anhydrous sodium sulfate
- distillationto distill off the solvent
- customThe residue was purified by silica gel column chromatography
出典と根拠
- ORDレコード
- ord-7d95fe21a8454b3185a13827bafa3bbc
- 出典データセット
- uspto-grants-1993_01
- 特許番号
- US05180836
反応ノート
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