HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → 2-[(Acetyloxy)methyl]4-(2-chloroethoxy)-5-methoxybenzyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-(2-Chloroethoxy)-4,5-bis(chloromethyl)-2-methoxybenzene | HCID 11716140 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-[(Acetyloxy)methyl]4-(2-chloroethoxy)-5-methoxybenzyl acetate | HCID 11587975 | 86% |
Reaction Steps
To a solution of 5.67 g (20 mmol) of 36 in 75 mL of acetic acid was added a solution of 3.5 g of anhydrous sodium acetate (42.7 mmol) in 100 mL of acetic acid. This mixture was refluxed with stirring for 2 h. Solids were removed by filtration and washed with acetic acid. The filtrate was evaporated to approximately 30 mL, then poured into water and extracted with ether. The organic phase was washed with aqueous sodium carbonate, water, and brine. After drying over sodium sulfate, the solution was filtered and evaporated to give 5.69 g (86%) of 2-[(acetyloxy)methyl]-4-(2-chloroethoxy)-5-methoxybenzyl acetate (37) as a white solid, mp 79-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759339B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-d8574a2add784f29906a8129f6c6f30e |
| Source note | uspto-grants-2014_06 |