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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306834Generated: November 1, 2026

Triphenylphosphine → ethyl 2-((1S)-5-{2-[5-methyl-2-(4-methylphenyl)(1,3-oxazol-4-yl)]ethoxy}indanyl)acetate

https://huagongshe.com/reaction/2306834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiamideHCID 5353800—
Reactant2-[5-Methyl-2-(4-methylphenyl)-1,3-oxazol-4-yl]ethanolHCID 10775145—
Reactantethyl 2-[(1S)-5-hydroxy-2,3-dihydro-1H-inden-1-yl]acetateHCID 16110404—
SolventDichloromethaneHCID 6344—
Productethyl 2-((1S)-5-{2-[5-methyl-2-(4-methylphenyl)(1,3-oxazol-4-yl)]ethoxy}indanyl)acetateHCID 23529369—

Reaction Steps

A suspension of the ethyl [(1S)-5-hydroxy-2,3-dihydro-1H-inden-1-yl]acetate prepared in Example 135 (507.5 mg, 2.30 mmol), and 2-[5-methyl-2-(4-methylphenyl)-1,3-oxazol-4-yl]ethanol prepared in Example 10 (500 mg, 2.30 mmol), TMAD (792.6 mg, 4.60 mmol), and Ph3P (1.21 g, 4.60 mmol) in 15 mL anhydrous DCM was stirred at rt under Ar for 12 hours. DCM was removed under reduced pressure. Flash chromatograph of the residue over silica gel using 1% CH3CN/CH2Cl2gave ethyl 2-((1S)-5-{2-[5-methyl-2-(4-methylphenyl)(1,3-oxazol-4-yl)]ethoxy}indanyl)acetate (776.3 mg, 1.85 mmol, 80.5%). HPLC/MS (M+H)+ m/z 420.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828335B2
Source datasetuspto-grants-2004_12
ORD IDord-a692ec5288d4481cad3b3b6816b72d41
Source noteuspto-grants-2004_12