HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387537Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 59564912, compound
https://huagongshe.com/reaction/387537
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Tert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylate | HCID 54299041 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 59564912 | HCID 59564912 | 97% |
Reaction Steps
DIBAL-H (73.6 mL, 110.4 mmol) (1.5M in Toluene) was added portionwise to a solution of tert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylate (23.1 g, 108.3 mmol) in dry Et2O (200 mL) cooled to −78° C. The reaction was stirred for 1 hour at −78° C., allowed to warm to room temperature and stirred for 15 hours. The reaction was quenched with NH4OH (50 mL), stirred for 20 minutes, and then diluted with EtOAc (200 mL) and 0.5M Rochelle's Salt (100 mL). The layers were separated. The organic fraction was washed with 0.5M Rochelle's (2×100 mL), brine (100 mL), dried (MgSO4) and concentrated to an oil. The oil was taken up in a solution of p-TsOH monohydrate (2.0 g, 10.8 mmol) in MeOH (200 mL) and stirred for 15 hours at room temperature. The reaction was concentrated, taken up in EtOAc (200 mL), washed with saturated Na2CO3 (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated to an oil, tert-butyl 5-methoxy-2,2-dimethylpyrrolidine-1-carboxylate (24.1 g, 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372842B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-e7312667e5aa40678085076d330b54ca |
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| Source note | uspto-grants-2013_02 |
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