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3,5-Dichlorobenzoyl chloride → 3,5-dichloro-N'-[4-(octyloxy)benzoyl]benzohydrazide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,5-Dichlorobenzoyl chloride | HCID 76191 | — |
| 反応物 | 2-(2,5-Dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole | HCID 21982073 | — |
| 生成物 | 3,5-dichloro-N'-[4-(octyloxy)benzoyl]benzohydrazide | HCID 21982109 | 60% |
反応手順
By the general method for the synthesis of 2-(2,5-dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole (1) in Example 3, the reaction of 3,5-dichlorobenzoyl chloride (20.0 g, 0.010 mole) with 4-octoxybenzoyl hydrazide (25.24 g, 0.010 mole) gave the intermediate 3,5-dichloro-N′-[4-(octyloxy)benzoyl]benzohydrazide (25 g, 60% yield). Cyclocondensation of the intermediate 3,5-dichloro-N′-[4-(octyloxy)benzoyl]-benzohydrazide (16.0 g) with POCl3 (83 mL) gave the required 2-(3,5-dichlorophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole (4) (11.16 g, 73% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07094902B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-7768084908b14dee8441d1827dd3fcea |
| 出典メモ | uspto-grants-2006_08 |