Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Butyl salicylate | HCID 16330 | — |
| Reactant | HCID 54165239 | HCID 54165239 | — |
| Reactant | Tricaprylylmethyl ammonium chloride | HCID 77620884 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53781625 | HCID 53781625 | — |
Reaction Steps
A 5.8 g portion of n-butyl salicylate was added to a solution of 1.2 g of sodium hydroxide in 75 ml of water, producing a thick suspension. To the above suspension was added 100 ml of methylene chloride and 0.3 g of tricaprylylmethyl ammonium chloride. The reaction mixture was stirred vigorously while a solution of 8.1 g of methyl N-[[N-[(fluorocarbonyl-N-methylamino)thio]-N-methylaminocarbonyloxy]]ethanimidothioate in 50 ml methylene chloride was added dropwise. When addition was complete, stirring was continued for one hour. The organic phase was separated and washed with 200 ml of water followed by 100 ml of saturated sodium chloride solution. The organic solution was dried over anhydrous magnesium sulfate, and the solvent was distilled under reduced pressure. On scratching and standing, the crude reaction product partially solidified. The title compound was isolated by dissolving the crude reaction product in 25 ml of ethanol, cooling the solution and diluting with hexane to afford 5.7 g of 2-[N-methyl-N-[N-methyl-N-[(1-methylthioethylidene)aminooxycarbonyl]aminothio]aminocarbonyloxy]benzoic acid butyl ester, m.p. 87° -89° C. Absorption bands characteristic of the title compound were observed in the infrared and NMR spectrums.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04210668 |
|---|
| Source dataset | uspto-grants-1980_07 |
|---|
| ORD ID | ord-9554b45789b843ec85959857526d640f |
|---|
| Source note | uspto-grants-1980_07 |
|---|