HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188031Generated: October 31, 2026
Acetyl chloride → Methyl 3-hydroxy-2-methylbenzoate
https://huagongshe.com/reaction/2188031
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Hydroxy-2-methylbenzoic Acid | HCID 252023 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-hydroxy-2-methylbenzoate | HCID 12488879 | 91% |
Reaction Steps
3-Hydroxy-2-methylbenzoic acid (0.5 g, 3.2 mmol) was dissolved in HPLC grade methanol (5 ml) and cooled to 0° C. under nitrogen. Acetyl chloride (5 ml) was added dropwise. Once the addition was complete, the ice bath was removed and the reaction mixture allowed warming to room temperature over a period of 18 hours. The reaction was complete by tlc (Rf=0.5, 1:1 ethyl acetate/hexanes) and quenched with saturated sodium bicarbonate. The reaction mixture was concentrated, diluted with dichloromethane and water and the layers separated. The aqueous layer was extracted with dichloromethane (3×). The organic layers were combined, dried (MgSO4), filtered and concentrated in vacuo, which afforded 0.5 g (91%) of 3-hydroxy-2-methylbenzoic acid methyl ester as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06410556B1 |
|---|
| Source dataset | uspto-grants-2002_06 |
|---|
| ORD ID | ord-a06a79e815914423b5a4c9f7df745283 |
|---|
| Source note | uspto-grants-2002_06 |
|---|