HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → 2-Allyloxy-tetrahydro-furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | 4-Hydroxybutanal | HCID 93093 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Allyloxy-tetrahydro-furan | HCID 524381 | 93% |
Reaction Steps
The procedure of Example 1 is followed with 4-hydroxybutanal (20.0 g of 11.5 wt. % solution, 26 mmol, 1.0 eq.), allyl alcohol (3.26 g, 56 mmol, 2.2 eq.), and hexanes (50 mL). Concentrated hydrochloric acid (2 drops) is used in place of the ion-exchange resin. After 3 h of stirring at room temperature, the hexane phase contains 8.8% of 2-allyloxytetrahydrofuran (3.1 g, 92.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254702 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-6a3e1472f9c44701921563b0217e587b |
| Source note | uspto-grants-1993_10 |