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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057413Generated: October 30, 2026

Sodium Hydroxide → HCID 53781625, compound

https://huagongshe.com/reaction/2057413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantButyl salicylateHCID 16330—
ReactantHCID 54165239HCID 54165239—
ReactantTricaprylylmethyl ammonium chlorideHCID 77620884—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 53781625HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04210668
Source datasetuspto-grants-1980_07
ORD IDord-9554b45789b843ec85959857526d640f
Source noteuspto-grants-1980_07