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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352117Generated: November 2, 2026

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

https://huagongshe.com/reaction/2352117

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 tetrahydrofuran (10 ml) was added dropwise. The resulting solution was stirred for 30 minutes after which a solution of 2-(8-phenyloctyl)benzaldehyde in tetrahydrofuran hydrofuran (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 numberUS04874792
Source datasetuspto-grants-1989_10
ORD IDord-8593657f7cef4136b3b8ca066f71dc58
Source noteuspto-grants-1989_10