HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474012Generated: October 29, 2026
Diisobutylaluminumhydride → HCID 59420732, compound
https://huagongshe.com/reaction/474012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 59420852 | HCID 59420852 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59420732 | HCID 59420732 | 32% |
Reaction Steps
Diisobutyl aluminium hydride (1.48 mmol, 1.48 ml, 1 M DCM) was added dropwise to a solution of tert-butyl 3-(2-(ethoxycarbonyl)ethyl)-3-hydroxyazetidine-1-carboxylate (0.10 g, 0.37 mmol) in DCM (3 ml) at −78° C. The solution was allowed to warm to 0° C. and stirred for a further 5 hrs. The reaction was quenched with Sat NH4Cl (10 ml) and extracted into ethyl acetate (10 ml), dried (Na2SO4), and concentrated to give an oil. The oil was purified by flash column chromatography eluting with 60% ethylacetate/hexanes to give the title compound as a colorless oil 27 mg, 32%. 1H NMR (CDCl3, 400 MHz) 1.48 (9H, s), 1.69-1.75 (2H, m), 1.93 (2H, t), 3.76 (2H, t), 3.82 (4H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637511B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-97ee65e145614e30aa36eb0caa6fc4c6 |
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| Source note | uspto-grants-2014_01 |
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