HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 19697534, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | HCID 19697600 | HCID 19697600 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19697534 | HCID 19697534 | — |
Reaction Steps
1.9 g of 4-tert-butoxycarbonyl-2(R,S)-hydroxymethyl-3,4-dihydro-2H1,4-benzothiazine are dissolved in 20 ml of tetrahydrofuran, and 1.5 g of a 20% potassium hydride suspension in oil are added at 0° C. 1.3 ml of methyl iodide are then added dropwise. The mixture is allowed to warm to room temperature and, when the reaction has ended, the mixture is poured onto water. After customary working up, the crude product is purified over 250 g of silica gel by means of FC (methylene chloride as the mobile phase): Rf (D)=0.45.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719141 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-be4e586e8bd44aedbc05f5ed534b568c |
| Source note | uspto-grants-1998_02 |