関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Triethylamine hydrochloride | HCID 11130 | — |
| 反応物 | Sodium Azide | HCID 33557 | — |
| 反応物 | 4-(Benzyloxy)-2-methoxybenzonitrile | HCID 22591720 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5-[4-(benzyloxy)2-methoxyphenyl]-2H-tetrazole | HCID 22591718 | — |
反応手順
A vigorously stirred suspension of 4-benzyloxy-2-methoxybenzonitrile (1-B) (1.20 g, 5.0 mmol), sodium azide (732 mg, 11.3 mmol), and triethylamine hydrochloride (1.54 g, 11.3 mmol) in toluene (6 mL) was heated at 110° for 48 h. The brown suspension was cooled, water (15 mL) was added, and the mixture stirred for 30 min. The organic layer was separated and extracted with water (5 mL). The combined aqueous extracts were acidified to about pH 1 with concentrated HCl. The gum that initially precipitated solidified upon stirring for 30 min. The solid was filtered, washed with water, and dried to give 5-[4-(benzyloxy)2-methoxyphenyl]-2H-tetrazole (1-C). 1H NMR (500 MHz, CDCl3): δ 12.9 (vbs, 1H), 7.37 (d, 1H, J=8.7 Hz), 7.34-7.48 (m, 5H), 6.78 (dd, 1H, J=2.3, 8.7 Hz), 6.70 (d, 1H, J=2.3 Hz), 5.15 (s, 2H), 4.05 (s, 3H) ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06849636B2 |
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| 出典データセット | uspto-grants-2005_02 |
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| ORD ID | ord-d7f602c1d4704f5585847a823c360e27 |
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| 出典メモ | uspto-grants-2005_02 |
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