HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596493Generated: October 25, 2026
Formaldehyde → 1-Benzoylethylene dimethyldithiocarbamate
https://huagongshe.com/reaction/596493
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Dimethyldithiocarbamic acid, dimethylamine | HCID 11728 | — |
| Reactant | 2-Oxo-2-phenylethyl dimethylcarbamodithioate | HCID 238111 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzoylethylene dimethyldithiocarbamate | HCID 86734534 | — |
Reaction Steps
A solution of phenacyl dimethyldithiocarbamate (12.0 grams, 0.050 mole), formaldehyde (4.1 grams of 37% aqueous solution, 0.050 mole), carbon disulfide (1.9 grams, 0.025 mole), and dimethylammonium dimethyldithiocarbamate (8.3 grams, 0.050 mole) in methanol (50 ml.) was stirred and heated at 38° C.-40° C. for 2.5 hours. The reaction mixture was then cooled to 0° C. and the precipitated product was filtered off, washed with cold methanol and dried in air. The yield of product melting at 106° C.-108.5° C. was 17.6 grams (94%). Repeated recrystallization from methylene chloride-methanol and acetone-2-propanol solution without heat gave pure 1-benzoylethylene dimethyldithiocarbamate melting at 106° C.-109.5° C. The structure was determined from the infrared spectrum and elemental analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011230 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-c229064febd34a56ba134c21af52d765 |
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| Source note | uspto-grants-1977_03 |
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