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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625689Generated: October 30, 2026

4-Benzyloxy-3-fluorophenylboronic Acid → (1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-3-fluoro-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/625689

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-3-fluorophenylboronic AcidHCID 2737788—
Reactant(1S,2S)-2-[4-((R)-7-Fluoro-4-hydroxy-indan-1-yloxy)-phenyl]-cyclopropanecarboxylic acid ethyl esterHCID 118093712—
Reactant(1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl esterHCID 118093741—
Product(1S,2S)-2-{4-[(R)-4-(4-Benzyloxy-3-fluoro-phenoxy)-7-fluoro-indan-1-yloxy]-phenyl}-cyclopropanecarboxylic acid ethyl esterHCID 118093721—

Reaction Steps

The title compound is prepared from (1S,2S)-2-[4-((R)-7-fluoro-4-hydroxy-indan-1-yloxy)-phenyl]-cyclopropanecarboxylic acid ethyl ester (Intermediate 5, 0.8 g, 2.2 mmol) and 4-benzyloxy-3-fluorophenylboronic acid (2.21 g, 9.0 mmol) in a manner analogous to that described for Intermediate 6 (Yield 0.8 g). LC (METHOD 6): tR=0.96 min; Mass spectrum (ES+): m/z=557 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09308194B2
Source datasetuspto-grants-2016_04
ORD IDord-02a3185c6cc942c0b4266d7051898366
Source noteuspto-grants-2016_04