HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265697Generated: October 25, 2026
Pivalaldehyde → 3-(2,2-Dimethylpropylideneamino)-pyrrolidine
https://huagongshe.com/reaction/265697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | 3-Aminopyrrolidine | HCID 164401 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(2,2-Dimethylpropylideneamino)-pyrrolidine | HCID 14836604 | 74% |
Reaction Steps
34.5 g (0.4 mol) of 3-aminopyrrolidine are initially introduced into 100 ml of toluene, and 34.5 g (0.3 mol) of 75% strength pivalaldehyde (preparation from Riedel-de-Haen) in 100 ml of toluene are added dropwise at 20° C., while cooling in a water bath. The mixture is subsequently stirred at room temperature for 2 hours, the aqueous phase is then separated off in a separating funnel (4.6 ml) and the toluene solution is dried over sodium sulphate for 1 hour. The toluene is separated off on a rotary evaporator and the residue is distilled using a small Vigreux column. 46.2 g of 3-(2,2-dimethylpropylideneamino)-pyrrolidine of boiling point 61° C./10 mbar are obtained with a purity, determined by gas chromatography, of 98%, corresponding to a yield of 74% and a selectivity of 99% (pivalaldehyde).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648493 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-4c1a66e4a85044c985a27efcecdb09d2 |
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| Source note | uspto-grants-1997_07 |
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