HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → alpha-(Nitromethyl)benzyl dimethyldithiocarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Dimethyldithiocarbamic acid, dimethylamine | HCID 11728 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-(Nitromethyl)benzyl dimethyldithiocarbamate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148795 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-b12af338d5e445109bf46b1ee5d17697 |
| Source note | uspto-grants-1979_04 |