HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Methyl 5-acetyl-2,4-dihydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | 4-Acetoxy-2-hydroxy-benzoic acid methyl ester | HCID 57990217 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 5-acetyl-2,4-dihydroxybenzoate | HCID 12482079 | — |
Reaction Steps
The toluene solution from Step 1 was cooled in an ice bath under N2 and triflic acid (9.44 L) added slowly over 3 h. On stirring a fine white solid was formed which dissolved on warming to RT over 20 h and then stirring at RT for 37 h to give a yellow solution. To the solution was added acetyl chloride (726 mL) and the solution stirred at RT for a further 1 h. This solution was cannulated into a stirred cooled (0° C.) solution of EtOAc (217.8 L) and NaOAc.3H2O (14.52 Kg) dissolved in water (145 L). The organic phase was washed with saturated brine (twice, 72.6 L), and was evaporated to 5.5 Kg. Toluene: Isopropanol (2:3) was added and the crystalline solid removed by filtration and dried to give 12.6 Kg (61% over 2 steps), mp 124-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428439B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-3d3dc3a026dd4b80a4a2653308ec358b |
| Source note | uspto-grants-2016_08 |