HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Methyl 4-(chloromethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 4-(hydroxymethyl)benzoate | HCID 81325 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-(chloromethyl)benzoate | HCID 36664 | 81.5% |
Reaction Steps
To a solution of p-methoxycarbonylbenzyl alcohol (332.0 g, 2.0 mol) in methylene chloride (600 mL) is added thionyl chloride (380 g, 3.2 mol) dropwise over 3 hours and the reaction mixture heated at gentle reflux for 6 hours, allowing excess gases to escape. The excess thionyl chloride and methylene chloride are removed and the yellow oil triturated with hexane to yield a total of 300 g (81.5% yield) of white, solid methyl α-chloro-p-toluate, the identity of which is confirmed by elemental analysis and mass spectrum analysis as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845187 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-e1acda5dda51424f85d303f1dbac3770 |
| Source note | uspto-grants-1989_07 |