HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → Methyl 5-(chloromethyl)-2-methoxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 5-(hydroxymethyl)-2-methoxybenzoate | HCID 18465013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(chloromethyl)-2-methoxybenzoate | HCID 240622 | — |
Reaction Steps
Combine methyl 2-methoxy-5-hydroxymethylbenzoate (1.34 g, 6.8 mmol) and N,N-diisopropylethylamine (1.4 mL) in dichloromethane (25 mL). Cool in a ice-bath. Add dropwise, methanesulfonyl chloride (0.56 mL). After 30 minutes, warm to ambient temperature. After 2 hours, dilute with dichloromethane and extract with 1 M hydrochloric acid solution and 5% sodium bicarbonate solution. Dry the organic layer over Na2SO4, filter, and concentrate in vacuo to give methyl 2-methoxy-5-chloromethylbenzoate: Rf=0.64 (silica gel, 1/1 ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211199B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-b1fe6c8543724b74ac46d56b5eb48e09 |
| Source note | uspto-grants-2001_04 |