HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Benzyloxy-3-methylcarbonyl-1-(2,3-epoxypropoxy) Benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 57143294 | HCID 57143294 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Benzyloxy-3-methylcarbonyl-1-(2,3-epoxypropoxy) Benzene | HCID 17887084 | — |
Reaction Steps
A solution containing 1 g (0.0048 mole) of the product of example 39, 0.856 ml (0.00072 mole) of benzyl bromide and 0.924 g (0.0072 mole) of K2CO3 in 12 ml of acetone are heated for 6 hours under reflux in nitrogen. Then 0.5 ml (0.0042 mole) of benzyl bromide are added and the mixture heated for a further 7 hours. The substance is poured into water, extracted with ethyl acetate and the solvent evaporated off . The reaction product is purified by chromatography, eluting with an 8/2 mixture of hexane and acetone. The required product is obtained, MP: 45-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649627B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-f0deee0d8285412697561ff1f9d7edb9 |
| Source note | uspto-grants-2003_11 |