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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56579Generated: October 28, 2026

Diisobutylaluminum hydride → HCID 58432110, compound

https://huagongshe.com/reaction/56579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantN,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamideHCID 58431993—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 58432110HCID 58432110105.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of N,2-dimethoxy-N-methyl-2-(4-morpholinophenyl)acetamide (1.5 g, 5.1 mmol) in anhydr CH2Cl2 (12 mL) and anhydr toluene (6 mL) at −78° C. was added a solution of DIBALH (1 M in hexanes, 7.8 mL, 7.8 mmol) dropwise over 5 min. After stirring at −78° C. for 1 hr, the reaction was quenched with the dropwise addition of EtOAc. The mixture was stirred 2 min then Et2O and saturated aqueous NH4Cl were added and the mixture was warmed to room temp. After stirring for 30 min the mixture was diluted with EtOAc and H2O and the layers separated. 10% Aqueous potassium sodium tartrate was added to the aqueous layer and it was extracted with EtOAc/Et2O. The combined organics were washed with saturated aqeuous NH4Cl and dried over Na2SO4 to give 2-methoxy-2-(4-morpholinophenyl)acetaldehyde as a yellow oil (1.27 g). The product was used in the next synthetic step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434707B2
Source datasetuspto-grants-2016_09
ORD IDord-7e877c0feca74c439ff6357d35b3f749
Source noteuspto-grants-2016_09