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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403408Generated: October 31, 2026

1-Tert-butyl 2-methyl pyrrolidine-1,2-dicarboxylate → 1-Boc-2-Formylpyrrolidine

https://huagongshe.com/reaction/2403408

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butyl 2-methyl pyrrolidine-1,2-dicarboxylateHCID 394147—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTolueneHCID 1140—
Product1-Boc-2-FormylpyrrolidineHCID 422781588.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (3.5 g) in toluene (40 mL) at −78° C. was added dropwise diisobutylaluminium hydride (20 mL of a 1.5 M solution in toluene) maintaining the temperature below −65° C. The reaction mixture was stirred at −78° C. for 2 h and then quenched with methanol (10 mL). The mixture was then diluted with diethyl ether (50 mL), potassium sodium tartrate tetrahydrate was added and the mixture stirred vigorously for 20 min at room temperature. The two phases were then separated and the aqueous layer extracted with dichloromethane (2×50 mL). The combined organics were then washed with brine (100 mL), dried (MgSO4), reduced in vacuo and purified by column chromatography to give 2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a pale yellow oil (2.687 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802670B2
Source datasetuspto-grants-2014_08
ORD IDord-11963fdbc1af4c28be0159d9768902a5
Source noteuspto-grants-2014_08