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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919281Generated: November 1, 2026

Trichloromethanesulfenyl chloride → HCID 13193083, compound

https://huagongshe.com/reaction/1919281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloromethanesulfenyl chlorideHCID 11666—
ReactantSodium HydroxideHCID 14798—
ReactantPropanimidamide, 2,2-dimethyl-, hydrochloride (1:1)HCID 2781880—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 13193083HCID 1319308360%

Reaction Conditions

Temperature-15 °C

Reaction Steps

6.83 g (50.00 mmol) of tert-butylcarbamidine hydrochloride are dissolved in 60 ml of dichloromethane and treated with 8.37 g (45.00 mmol) of trichloromethanesulphenyl chloride, before the reaction mixture is cooled to −15° C. A solution of 10.00 g (250 mmol) of sodium hydroxide in 20 ml of water is added dropwise and the mixture obtained is stirred at AT for 3 h. After adding 50 ml of dichloromethane, extracting three times with water and drying the combined organic phases over MgSO4, the solvent is evaporated under vacuum. (5.81 g, 90% purity, 60% yield, log P (pH 2.3)=3.44).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168567B2
Source datasetuspto-grants-2012_05
ORD IDord-6ecfca2cb2f4480d83dd78ee9f3ae4c0
Source noteuspto-grants-2012_05