HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl Methyl Ether → 3-Chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Benzoyloxy-2-chloro-6-methylphenol | HCID 18504588 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene | HCID 18504633 | 96% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Then, 25 g of 4-benzoyloxy-2-chloro-6-methylphenol was dissolved in 250 ml of chloroform, to which 12 g of chloromethyl methyl ether was added, while stirring at 0° C., and 21 g of N-ethyldiisopropylamine was added dropwise. After heating under reflux for 1 hour, the chloroform layer was washed with water, and concentrated. The residue was subjected to silica gel chromatography, which afforded 27.4 g of 3-chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene (96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376428B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-d3f0aacf39eb4c08a6d620dbaa3ea39b |
| Source note | uspto-grants-2002_04 |