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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625688Generated: October 30, 2026

(1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester → (1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/625688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl esterHCID 118093741—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Product(1S,2S)-2-{4-[(R)-7-Fluoro-4-(4-hydroxy-phenoxy)-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl esterHCID 118093735—

Reaction Steps

(1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester (Intermediate 6, 0.76 g, 1.3 mmol) is dissolved in 1:1 MeOH/ethyl acetate (20 mL) and hydrogenated at 2 Bar for 1 hour using 10% palladium on carbon as the catalyst. The mixture is filtered through CELITE filter aid and the solvent removed under vacuum the title compound. (Yield 0.60 g). LC (METHOD 6): tR=0.64 min; Mass spectrum (ES+): m/z=449 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308194B2
Source datasetuspto-grants-2016_04
ORD IDord-975d16e7d0cc47b583a7298dade4f7f9
Source noteuspto-grants-2016_04