HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furfural → 1-(Furan-2-yl)but-3-en-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Bromide | HCID 25514 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Furan-2-yl)but-3-en-1-ol | HCID 253052 | — |
Reaction Steps
Reaction and after-treatment were carried out in the same manner as in Example 3 except that an equimolar amount of furfural was used in place of 5-methylfurfural, and that ammonium bromide and tetrahydrofuran were used in place of ammonium chloride and toluene, respectively, in the same weights as those of the latter, to obtain 50.6 g of the fraction of 2-(1-hydroxy-3-butenyl)-furan (content, 99.3%) (yield, 91.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05008410 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-f18e2fa4f5364ee6bc6a5b4e1034cc19 |
| Source note | uspto-grants-1991_04 |