関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | 3,5-Bis(trifluoromethyl)benzaldehyde | HCID 136247 | — |
| 反応物 | 2-methyl-2H-1,2,3,4-tetrazol-5-amine | HCID 138677 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5-[N-(3',5'-Bistrifluoromethylbenzyl)amino]-2-methyltetrazole | HCID 23073221 | 87.6% |
反応手順
A mixture of 3,5-bis(trifluoromethyl)benzaldehyde (4 g, 16.5 mmol), 2-methyl-2H-tetrazol-5-amine (1.96 g, 19.8 mmol) and molecular sieves (5-10 Å beads) in toluene (50 mL) was heated at reflux for 4 hours, after which time the solvent was removed. Ethanol (50 mL) and sodium borohydride (1.25 g, 33 mmol) were added. The resulting mixture was stirred at room temperature for 30 minutes and then partitioned between saturated NH4Cl (50 mL) and ethyl acetate (2×50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4), filtered and concentrated to yield the title compound as a white solid (4.7 g). 1H NMR (400 MHz, CDCl3) δ 4.2 (s, 3 H) 4.7 (s, 1 H) 4.7 (s, 1 H) 5.0 (t, J=6.0 Hz, 1 H) 7.8 (s, 1 H) 7.9 (s, 2 H). MS (ES+) Calc: 325.08, Found: 325.8 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08383660B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-63ad3bc616ff479fa3780317a102f092 |
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| 出典メモ | uspto-grants-2013_02 |
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