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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596494Generated: October 30, 2026

Benzaldehyde → alpha-(Nitromethyl)benzyl dimethyldithiocarbamate

https://huagongshe.com/reaction/596494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantCarbon DisulfideHCID 6348—
ReactantNitromethaneHCID 6375—
ReactantDimethyldithiocarbamic acid, dimethylamineHCID 11728—
SolventEthanolHCID 702—
Productalpha-(Nitromethyl)benzyl dimethyldithiocarbamateHCID 21324598—

Reaction Steps

A solution of dimethylammonium dimethyldithiocarbamate (16.6 grams, 0.10 mole), carbon disulfide (7.6 grams, 0.10 mole), benzaldehyde (21.2 grams, 0.20 mole), and nitromethane (9.2 grams, 0.15 mole) in 95% ethanol (50 ml.) was allowed to stand at 23° C. for several days. The resulting precipitate was filtered off, washed with cold 95% ethanol, and dried in air. The solid product, which melted at 101° C.- 102° C., was recrystallized from 2-propanol to give α-(nitromethyl)benzyl dimethyldithiocarbamate melting at 105° C.-106° C. The structure was determined from infrared and nuclear magnetic resonance spectra and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011230
Source datasetuspto-grants-1977_03
ORD IDord-0ff59a3980ab44ef9cf61ce9a3a2869d
Source noteuspto-grants-1977_03