HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283681Generated: October 25, 2026
Dibromomethane → Potassium diphenylmethyldithiocarbamate
https://huagongshe.com/reaction/1283681
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 1 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 | US03975528 |
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| Source dataset | uspto-grants-1976_08 |
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| ORD ID | ord-3f8d2385760a4777bcf761238cb68fcb |
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| Source note | uspto-grants-1976_08 |
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