HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 131717378, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 15078318 | HCID 15078318 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131717378 | HCID 131717378 | — |
Reaction Steps
Methanesulfonyl chloride (0.097 mL, 1.25 mmol) was added to a solution of trans-2-[3-(2-hydroxyethylsulfonyl)-4,5-di-n-propoxyphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran (338 mg, 0.63 mmol) in dichloromethane (3 mL) and pyridine (1.3 mL). The reaction mixture was stirred at room temperature for 2 h, and worked-up as usual to give a syrup, Rf 0.52 (hexane-ethyl acetate; 1:2 v/v). This material was used directly in the next experiment without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05114961 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-7d60563fc02e49918cbf64423b021ab9 |
| Source note | uspto-grants-1992_05 |