HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanesulfonyl chloride → 3,4,5-Trimethoxybenzyl Mesylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 3,4,5-Trimethoxybenzyl alcohol | HCID 77449 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3,4,5-Trimethoxybenzyl Mesylate | HCID 18464591 | — |
Reaktionsschritte
Combine 3,4,5-trimethoxybenzyl alcohol (9.0 g, 45.4 mmol), N,N-diisopropylethylamine (12.9 g, 100 mmol), and acetonitrile (60 mL). Cool in an ice bath. Add methanesulfonyl chloride (6.76 g, 49.0 mmol). After 2 hours, partition the reaction mixture between water and ethyl acetate. Separate the layers and extract the organic layer with 1 M hydrochloric acid solution and them a saturated solution of sodium bicarbonate. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06211199B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-fe813033fcf14a04924600f0eb5e1006 |
| Quellennotiz | uspto-grants-2001_04 |