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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087345Generated: October 26, 2026

Diisopropylamine → Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoate

https://huagongshe.com/reaction/1087345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantMethyl methoxyacetateHCID 80507—
Reactant2-(8-Phenyloctyl)benzaldehydeHCID 9817613—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl]propanoateHCID 15617503—

Reaction Steps

To tetrahydrofuran (50 ml), cooled to -78° C. under argon, was added diisopropylamine (5.7 ml, 0.041 mole) followed by n-butyllithium (16 ml, 0.041 mole) slowly. After 15 minutes, methyl methoxyacetate (4.25 g, 0.041 mole) in tetrhydrofuran (10 ml) was added dropwise. The resulting solution was stirred for 30 minutes after which a solution of 2-(8-phenyloctyl)benzaldehyde in tetrahydrofuran (10 ml) was added dropwise. After 2 hours the reaction mixture was quenched with a solution of saturated ammonium chloride and then diluted with ice water. The aqueous layer was extracted with ether. The combined ether extract was washed with 10% sodium hydroxide (ice cold), dried over magnesium sulfate, filtered and evaporated to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034537
Source datasetuspto-grants-1991_07
ORD IDord-13be1b05c4c14dac9708216186f5e413
Source noteuspto-grants-1991_07