Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539192생성일: 2026년 10월 25일
Lithium Hydroxide → 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid
https://huagongshe.com/reaction/539192
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lithium Hydroxide | HCID 3939 | — |
| 반응물 | methyl 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylate | HCID 67102198 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylic acid | HCID 56959981 | 69.1% |
반응 단계
To a mixture of methyl 1-[(3,4-dimethylphenyl)methyl]-2-methyl-6-(4-morpholinyl)-1H-benzimidazole-4-carboxylate (0.24 g, 0.61 mmol) in Tetrahydrofuran (THF) (10 mL) was added in lithium hydroxide (5.99 mL, 11.99 mmol). The reaction was stirred at 50° C. for 2 h. The reaction was cooled to room temperature. The organic solvent was removed in-vacuo. The precipitate was collected by filtration. Water (20 mL) was added in. The mixture was acidified with 1 N HCl. The resulting solid was filtered and washed with water and dried to give the product (0.16 g, 66%). 1H NMR (400 MHz, DMSO-d6) δ ppm 2.18 (s, 6H), 2.58-2.75 (s, 3H), 3.06-3.22 (m, 4H), 3.71-3.82 (m, 4H), 5.55 (s, 2H), 6.94 (m, 1H), 7.04 (s, 1H), 7.11 (d, 1H, J=7.83 Hz), 7.52 (m, 2H). MS (ES+) m/e 380.2[M+H]+
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08865912B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-6195b8639061401181af5e1d26b94cc6 |
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| 출처 메모 | uspto-grants-2014_10 |
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