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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683405Generated: October 31, 2026

Diisobutylaluminum hydride → HCID 22860777, compound

https://huagongshe.com/reaction/1683405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 12968270HCID 12968270—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 22860777HCID 2286077788.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3.72 g (13.9 mmol) of 4-benzyl-3-(R)-phenyl-2-morpholinone, prepared from (R)-phenyl-glycine as described in Example 14, in 28 mL of CH2Cl2 was cooled in a -78° C. bath under a N2 atmosphere and 14 mL of a 1.5M solution of DIBAL-H (21 mmol) in toluene were added. After stirring the resulting solution for 0.5 h, it was allowed to warm to -50° C. and mantained at this temperature for 0.5 h. The reaction mixture was quenched by adding 10 mL of aqueous potassium sodium tartarate. The mixture was diluted with CH2Cl2 and the layers were separated. The aqueous layer was extracted 3 times with CH2Cl2. The CH2Cl2 layers were washed with brine, dried over Na2SO4 and filtered. Concentration of the filtrate furnished 3.32 g (88%) of 4-benzyl-2-(S)-hydroxy-3-(R)-phenylmorpholine suitable for use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637699
Source datasetuspto-grants-1997_06
ORD IDord-a6e60ca4abdd4324bc24af5d2fccb3a0
Source noteuspto-grants-1997_06