HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661515Generated: November 3, 2026
Diisobutylaluminum hydride → HCID 86620859, compound
https://huagongshe.com/reaction/661515
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 66687263 | HCID 66687263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86620859 | HCID 86620859 | 59% |
Reaction Steps
To a stirred solution of 2-ethoxymethyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (1.00 g, 3.48 mmol, prepared using the procedure of preparation 3 step 1) in THF (40 mL) at −78° C. under nitrogen was added DIBALH (4.09 mL of 1.7 M solution in PhCH3, 6.96 mmol) dropwise over 15 minutes such that the internal temperature did not exceed −75° C. After 4.5 hours the reaction mixture was quenched by addition of sodium sulfate decahydrate (4 g) and MeOH (0.5 mL) and then warmed to ambient temperature. The reaction mixture was diluted with EtOAc (50 mL) and filtered. The filter cake was washed with EtOAc (200 mL), and the combined filtrates were concentrated in vacuo to a colourless oil. Purification by chromatography (silica, 10-30% EtOAc in hexanes) gave 2-ethoxymethyl-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester (0.528 g, 2.05 mmol, 59%) as a clear, colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084623B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-355afc7d222f4f1c829f07d0a2fb90dd |
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| Source note | uspto-grants-2011_12 |
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