HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Chloro-4-methoxybenzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (3-Chloro-4-methoxyphenyl)methanol | HCID 4312004 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-4-methoxybenzyl chloride | HCID 11159814 | 61.1% |
Reaction Steps
To a solution of 3-chloro-4-methoxybenzyl alcohol (1.1 g, 6 mmol) in tetrahydrofuran (5 mL) were added under ice-cooling triethylamine (1.67 mL, 12 mmol) and methanesulfonyl chloride (0.51 ml, 6 mmol) and the mixture was stirred at room temperature for 18 h. The solvent was evaporated under reduced pressure and the obtained residue was dissolved in ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give an almost pure title compound (700 mg, 61%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087597B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-e4e85b88e8b940a682a714ca09b108c4 |
| Source note | uspto-grants-2006_08 |