HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl N-[4-(benzothiazol-2-ylmethoxy)-2-methylphenyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 4-(Benzo(D)Thiazol-2-Ylmethoxy)-2-Methylaniline | HCID 935400 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl N-[4-(benzothiazol-2-ylmethoxy)-2-methylphenyl]carbamate | HCID 18932257 | 54% |
Reaction Steps
82.5 ml of pyridine and 18.9 ml of methyl chloroformate were added to a solution of 55.0 g of 4-(benzothiazol-2-ylmethoxy)-2-methylaniline [prepared as described in step (b) above] in 400 ml of dimethylformamide cooled in an ice-water bath and the resulting mixture was stirred at the same temperature for 2 hours. At the end of this time, the reaction mixture was poured into water resulting in the precipitation of a crystalline solid which was washed with water and then further washed with diethyl ether to give a crude crystalline solid. This was recrystallised from a 4:1 by volume mixture of tetrachloromethane and acetone to give 36.2 g (yield 54%) of the title compound as a solid having a melting point of 147° to 149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05736487 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-40fed1140ea944a284d72e6013d21908 |
| Source note | uspto-grants-1998_04 |