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Furfural → 11-(2-Furyl)-10-undecenoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Furfural | HCID 7362 | — |
| 反応物 | (9-Carboxynonyl)(triphenyl)phosphanium bromide | HCID 18795071 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 11-(2-Furyl)-10-undecenoic acid | HCID 54439232 | 59% |
反応手順
This compound was synthesized from 2-furaldehyde (1.92 g, 20 mmol) and 9-carboxynonyltriphenylphosphonium bromide (10.27 g, 20 mmol) in THF (100 mL) by a Wittig reaction. Crystallization (petroleum ether) afforded the product (2.95 g, 59%) as white crystals (mp 45-46° C.); IR: 3450-2500 cm-1 ; 1H-NMR: 1.33 (m, 8H), 1.46 (m, 2H), 1.65 (m, 2H), 2.34 (t, 2H), 2.45 (m, 2H), 5.55 (m, 1H), 6.18 (d, 1H), 6.25 (d, 1H), 6.38 (d, 1H), 7.38 (s, 1H), 9.80 (bs, 1H). Anal. Calcd. for C15H22O3 :C, 71.97, H, 8.86%; Found: C, 71.93, H, 8.87%. Z:E=43:57.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05998642 |
| 出典データセット | uspto-grants-1999_12 |
| ORD ID | ord-0a6d6843e84e437b8b48deec2cb6e18e |
| 出典メモ | uspto-grants-1999_12 |