HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 3-Bromo-4-ethoxybut-3-EN-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-Buten-2-one, 3-bromo-4-hydroxy- | HCID 57358789 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Bromo-4-ethoxybut-3-EN-2-one | HCID 53423743 | 100% |
Reaction Steps
A mixture of 400 ml absolute ethanol and 60 ml toluene was heated to reflux and 20 ml of azeotrope was removed via a Dean Stark trap. To the ethanol-toluene solution was added 33.0 g (0.2 mol) of 3-bromo-4-hydroxy-3-buten-2-one and reflux was continued for 2 hours during which period three aliquots of 20 ml of ethanol-toluene were removed via the trap. The solution was concentrated in vacuo to give 38.6 g (100%) of 3-bromo-4-ethoxy-3-buten-2-one as a mobile oil. nmr (DMSOd-6) (δ): 8.21 (s, 1H); 4.23 (q, 2H); 2.33 (s, 3H); 1.31 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04510313 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-21be4d1631a34d2999112bd66ab71e30 |
| Source note | uspto-grants-1985_04 |