HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131189Generated: October 30, 2026
Isobutyraldehyde → HCID 11300027, compound
https://huagongshe.com/reaction/131189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 4-Benzylmorpholin-3-one | HCID 12294087 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11300027 | HCID 11300027 | — |
Reaction Steps
To a stirred solution of 2 (5.05 g, 26.4 mmol) in tetrahydrofuran (25 ml) at −78° C. under nitrogen was added lithium diisopropylamide (14.5 ml of a 2M solution, 29.0 mmol) dropwise over 40 minutes. The reaction mixture was stirred at the same temperature over 30 minutes after which time a solution of isobutyraldehyde (2.63 ml, 29.0 mmol) in tetrahydrofuran (15 ml) was added dropwise over 30 minutes. After one hour, the reaction mixture was allowed to warm to room temperature and quenched by addition of saturated ammonium chloride solution. Extraction with dichloromethane and drying over magnesium sulphate gave 53 as a mixture of diastereomers. Upon concentration in vacuo one diastereomer precipitated as a white solid (53a: 0.99 g). The remaining mother liquors were purified by column chromatography (30% ethyl acetate in hexane [v/v]) to give 53 (2.06 g). MW 263.34; C15H21NO3; LCMS (6 min method): m/z 286 [M+Na]+; RT=2.748.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384941B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-d9b56de4fdf94651b96639cdaf7e1b1b |
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| Source note | uspto-grants-2008_06 |
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