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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625692Generated: October 30, 2026

Triphenylphosphine → (1S,2S)-2-(4-{(R)-7-Fluoro-4-[4-(2-morpholin-4-yl-ethoxy)-phenoxy]-indan-1-yloxy}-phenyl)-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/625692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant(1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl esterHCID 118093735—
SolventTetrahydrofuranHCID 8028—
Product(1S,2S)-2-(4-{(R)-7-Fluoro-4-[4-(2-morpholin-4-yl-ethoxy)-phenoxy]-indan-1-yloxy}-phenyl)-cyclopropanecarboxylic acid ethyl esterHCID 118093751—

Reaction Conditions

Temperature0 °C

Reaction Steps

(1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester (Intermediate 7, 140 mg, 0.29 mmol), N-(2-hydroxyethyl)morpholine (42 mg, 0.32 mmol), and triphenylphosphine (84 mg, 0.32 mmol) are suspended in dry tetrahydrofuran (5 mL) and cooled to 0° C. Di-tert-butyl azodicarboxylate (74 mg, 0.32 mmol) is added, the mixture is stirred for 2 hours at 0° C. then 2 h at room temperature. The solvent is removed under vacuum and residue is purified by flash chromatography (0-20% ethyl acetate in cyclohexane) to give the title compound. (Yield 175 mg, 55% content). LC (METHOD 6): tR=0.57 min; Mass spectrum (ES+): m/z=562 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308194B2
Source datasetuspto-grants-2016_04
ORD IDord-9b8d4a1bd48c4d91a50deba0434b3e3d
Source noteuspto-grants-2016_04