HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2,6-Dimethylbenzyloxy)-2-methoxybenzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 66959407 | HCID 66959407 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2,6-Dimethylbenzyloxy)-2-methoxybenzyl methanesulfonate | HCID 86657009 | — |
Reaction Steps
To a solution of (3-(2,6-dimethylbenzyloxy)-2-methoxyphenyl)methanol (Step B, 9.5 g, 32.7 mmol) and triethylamine (5.80 g, 57.4 mmol) in dry CH2Cl2 (100 ml) was added drop wise methanesulfonyl chloride (3.5 ml, 45 mmol) at 0° C. under argon. The reaction mixture was warmed to room temperature for 6 hours or until all the starting material is consumed, neutralized with cooled 10% Na2CO3 and extracted with CH2Cl2. The organic layer was concentrated, and purified by flash chromatography on a silica gel column (hex: methylene chloride 2:1) to give the title compound as light yellow oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889724B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-5efbc75b3aa648ffbfa85a2cc98cc9a5 |
| Source note | uspto-grants-2014_11 |