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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071813Generated: October 28, 2026

Methyl iodide → HCID 12458615, compound

https://huagongshe.com/reaction/2071813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantTriethylamineHCID 8471—
ReactantHCID 178449958HCID 178449958—
SolventEthanolHCID 702—
ProductHCID 12458615HCID 12458615—

Reaction Steps

2-Aminoethane-N-t-butylsulfonamide hydrochloride (1.25 g., 5.78 mmol.) was added to a solution of 1.17 g. (11.56 mmol.) of triethylamine in 20 ml. of ethanol. Carbon disulfide (0.44 g., 5.78 mmol.) was added, the mixture was stirred at 25° for 1.5 hours, then 0.82 g. (5.78 mmol.) of methyl iodide in 5 ml. of ethanol was added and the resulting mixture was stirred for 1.5 hours. The mixture was evaporated to dryness and the residue was dissolved in water and acidified to pH 2.0 with dilute hydrochloric acid. The aqueous mixture was extracted with ethyl acetate and the extract was dried (MgSO4) and evaporated to dryness to give methyl 2-(N-t-butylsulfamoyl)ethyldithiocarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04048311
Source datasetuspto-grants-1977_09
ORD IDord-cba943f9f45a4505900f633312d7a17a
Source noteuspto-grants-1977_09