HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596496Generated: October 26, 2026
Acetic Acid → 2-Nitro-1-phenylethyl pyrrolidine-1-carbodithioate
https://huagongshe.com/reaction/596496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Beta-Nitrostyrene | HCID 7626 | — |
| Reactant | Ammonium pyrrolidinedithiocarbamate | HCID 517348 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Nitro-1-phenylethyl pyrrolidine-1-carbodithioate | HCID 53637974 | 77% |
Reaction Steps
β-Nitrostyrene (7.5 grams, 0.050 mole) was added to a cooled (10° C.) stirred slurry of ammonium 1-pyrrolidinecarbodithioate (8.2 grams, 0.050 mole) in methanol (50 ml.). The temperature of the mixture fell to 5° C., then rapidly climbed to 10° C. The cooling bath was removed and the reaction temperature rose slowly to 22° C. Acetic acid (3.0 grams, 0.05 mole) was added, the slurry was cooled to 10° C. and the solid was filtered off, washed with water, and dried in air. The crude product melted at 108° C.-116° C. and weighed 11.4 grams (77% yield). Repeated recrystallizations from cool acetone-methanol, hot acetone-2-propanol, and cool methylene chloride-toluene-hexane solutions gave pure α-(nitromethyl)benzyl 1-pyrrolidinecarbodithioate melting at 116° C.-120° C. (sintering at 113° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04011230 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-00c918cd864944498c2b164262316541 |
|---|
| Source note | uspto-grants-1977_03 |
|---|