HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(Methoxy)-4-(benzyloxy)benzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Benzyloxy-3-methoxybenzyl alcohol | HCID 98832 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Methoxy)-4-(benzyloxy)benzyl methanesulfonate | HCID 57594645 | — |
Reaction Steps
A solution of 3-(methoxy)-4-(benzyloxy)benzyl alcohol (0.244 g, 1.00 mmol) in CH2Cl2 (2.0 mL) was treated with methanesulfonylchloride (0.085 mL, 1.10 mmol) and Et3N (0.160 mL, 1.15 mmol). After stirring 1 h at ambient temperature, the reaction mixture was filtered through a short plug of silica gel using CH2Cl2 as the eluant. The solution was concentrated in vacuo and taken on without purification. MS (ES+) m/e 323 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772507B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-d9d9cfa8f29c4b7e9be889d9b8217100 |
| Source note | uspto-grants-2014_07 |