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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040268Generated: 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/1040268

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 2352936980.5%

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/CH2Cl2 gave 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 numberUS08552203B2
Source datasetuspto-grants-2013_10
ORD IDord-e3e2c1af10b148858212c3308a285c8b
Source noteuspto-grants-2013_10