HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furfural → 12-(2-Furyl)-11-dodecenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Phosphonium, (10-carboxydecyl)triphenyl-, bromide | HCID 11432504 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 12-(2-Furyl)-11-dodecenoic acid | HCID 54228690 | 45% |
Reaction Steps
This compound was synthesized from 10-carboxydecyltriphenylphosphonium bromide (10.50 g, 20 mmol) and furfural (1.92 g, 20 mmol) in THF (100 mL) by a Wittig reaction. Crystallization afforded the product (2.38 g, 45%) as pale yellow crystals (mp 38-39° C.); IR: 3450-2500, 1715, 695 cm-1 ; 1H-NMR: 1.35 (m, 14H), 2.35 (t, 4H), 5.60 (m, 1H), 6.30 (m, 3H), 7.35 (s, 1H), 9.40 (bs, 1H). Anal. Calcd. for C16H24O3 : C, 72.69, H, 9.15; Found: C, 72.44, H, 9.06%. Z:E=43:57.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06025511 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-ceca8d936fe04640a47193c2a7ab8e9f |
| Source note | uspto-grants-2000_02 |