HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 1-[4-(3-Chloropropoxy)-2-hydroxy-5-methoxyphenyl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(2,4-Dihydroxy-5-methoxyphenyl)ethan-1-one | HCID 49850540 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[4-(3-Chloropropoxy)-2-hydroxy-5-methoxyphenyl]ethanone | HCID 18467243 | 70.3% |
Reaction Steps
A mixture of 2,4-dihydroxy-5-methoxyacetophenone (1.4 g, 7.7 mmol), K2CO3 (1.4 g, 10.0 mmol), 3-chlorobromopropane (1.6 g, 10.0 mmol) and acetone (25 mL) was stirred and refluxed under N2 for 16 hours. The reaction was poured into H2O, and the aqueous suspension was extracted with ethyl acetate. The extract was washed (H2O, brine) dried (MgSO4) and concentrated to yield 1.4 g of an off-white solid. Recrystallization twice from ethanol afforded 0.4 g of the alkylated phenol as a solid, m.p. 99°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05654319 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-37a8ed1b15064290b1de5e23f74a371b |
| Source note | uspto-grants-1997_08 |