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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644132Generated: November 2, 2026

Carbamic Acid → HCID 86618659, compound

https://huagongshe.com/reaction/1644132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamic AcidHCID 277—
ReactantDiethyldithiocarbamic AcidHCID 8987—
Reactant4-(Chloromethyl)benzoic acidHCID 74234—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 86618659HCID 8661865962%

Reaction Conditions

Temperature45 °C

Reaction Steps

4-Chloromethylbenzoic acid (4 g, 0.0234 mol, 1.0 equiv.) was dissolved in warm ethanol (20 mL). Diethyldithiocarbamic acid, sodium salt trihydrate (7.92 g, 0.0328 mol, 1.5 equiv.) was also separately dissolved in warm ethanol (20 mL). The solution of the carbamic acid was then added to the solution of the carboxylic acid. The resulting mixture was then stirred at 40-50° C. for 2 h, then stirred overnight at r.t. The reaction mixture was then evaporated to dryness and separated between dichloromethane and brine. The aqueous layer was separated and acidified with conc. HCl to a pH value of 2. The precipitate that formed on acidification was filtered and air-dried to give a white solid, 4.1 g (yield 62%). 1H NMR (acetone-d6, 400 MHz) δ 1.26, br.s, 6H, 2×CH3; 3.82, br.s, 2H, CH2N; 4.5, br.s, 2H, CH2N; 4.67, s, 2H, CH2S; 7.56 (d, J=8 Hz, 2H, aromatic); 7.98 (d, J=8 Hz, 2H, aromatic) ppm. 13C NMR (acetone-d6, 400 MHz) δ 11.78, 12.98, 41.53, 47.55, 50.45, 130.26, 130.45, 130.69, 143.74, 167.40, 194.94 ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124188B2
Source datasetuspto-grants-2012_02
ORD IDord-410feb6d50224b7ababab615e79dab68
Source noteuspto-grants-2012_02