HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596497Generated: October 25, 2026
Carbon Disulfide → alpha-(Nitromethyl)benzyl 1-piperidinecarbodithioate
https://huagongshe.com/reaction/596497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Beta-Nitrostyrene | HCID 7626 | — |
| Reactant | Piperidinium 1-piperidinecarbodithioate | HCID 2820349 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-(Nitromethyl)benzyl 1-piperidinecarbodithioate | HCID 11266906 | — |
Reaction Steps
β-Nitrostyrene (14.9 grams, 0.10 mole) was added in portions to a stirred mixture of piperidinium 1-piperidinecarbodithioate (24.6 grams, 0.10 mole), and carbon disulfide (7.6 grams, 0.10 mole) in methanol (200 ml.). During the addition, the reaction temperature was 25° C.-29° C. After the addition of β-nitrostyrene, the reaction mixture was cooled to 8° C., and the precipitated product was filtered off, washed with water, and dried in air. The yield of product melting at 85° C.-87° C. (prior sintering) was 29.0 grams (93%). Repeated recrystallizations without heating from methylene chloride-hexane and methylene chloride-methanol solutions gave pure α-(nitromethyl)benzyl 1-piperidinecarbodithioate melting at 86° C.-90.5° C. (prior sintering).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04011230 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-ae882f0193e946c4bdea7fcb06b2bf74 |
|---|
| Source note | uspto-grants-1977_03 |
|---|