HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 15044334, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | HCID 15917599 | HCID 15917599 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15044334 | HCID 15044334 | — |
Reaction Steps
One hundred ml of dichloromethane and 20.27 g (0.1 mol) of p-methylthiophenyl chloroformate prepared in the same manner as in Example 1 were placed in a flask, and 50 ml of a dichloromethane solution containing 8.15 g (0.1 mol) of tertamyl alcohol and 8.70 g (0.11 mol) of pyridine was dropped thereto at room temperature. The resulting mixture was then stirred for two hours. The reaction solution was washed with water to remove pyridine hydrochlorate, and the organic layer was concentrated under reduced pressure. Finally excessive pyridine was removed in vacuum whereupon 5.09 g of the desired product, tert-amyl p-methylthiophenyl carbonate was obtained as an oily material (yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05187311 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-3d76a7ca52104e1e8fc6034e75433416 |
| Source note | uspto-grants-1993_02 |