HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436627Generated: October 25, 2026
Dibromomethane → Potassium diphenylmethyldithiocarbamate
https://huagongshe.com/reaction/436627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Potassium bisulfide | HCID 102109 | — |
| Reactant | Benzhydryl isothiocyanate | HCID 520742 | — |
| Reactant | t-BuOH acetone | HCID 19966414 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Potassium diphenylmethyldithiocarbamate | HCID 23667332 | — |
Reaction Steps
Potassium diphenylmethyldithiocarbamate was prepared from diphenylmethyl isothiocyanate and potassium hydrosulfide in a t-butyl alcohol acetone mixture. A mixture of 29.7 g. of this salt, 26.1 g. of methylene bromide, and 10.1 g. of triethylamine in 200 ml. of dimethylformamide was stirred for about one hour keeping the initial reaction temperature below 30° C. by cooling. The mixture was poured into ice-water, partitioned into ethylene chloride, and gave 24.0 g. of crude product upon evaporation of the ethylene chloride. Purification by dry column chromatography on silica gel using 20% methylene chloride in hexane for developing gave 5.5 g. of solids which were recrystallized from isopropyl alcohol to give 4.4 g. of white crystals, m.p. 106.5°-107.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009279 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-7f3350bbf1df4667a479c36e7ae3cce7 |
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| Source note | uspto-grants-1977_02 |
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