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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406536Generated: October 30, 2026

{(S)-6-[(R)-4-bromo-5-cyano-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester → {(S)-6-[(R)-5-Cyano-4-(2,6-difluoro-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

https://huagongshe.com/reaction/2406536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{(S)-6-[(R)-4-bromo-5-cyano-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 86700771—
ReactantHCID 178505728HCID 178505728—
CatalystHCID 178439029HCID 178439029—
Product{(S)-6-[(R)-5-Cyano-4-(2,6-difluoro-benzyl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl esterHCID 86700801—

Reaction Steps

The title compound is prepared from {(S)-6-[(R)-4-bromo-5-cyano-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester and 2,6-difluoro-benzylzinc bromide following a procedure analogous to that described in Step 6 of Intermediate 1; [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]-(3-chloropyridyl)-palladium(II) dichloride (Pd-PEPPSI-IPr) is used as catalyst. LC (method 4): tR=1.22 min; Mass spectrum (ESI+): m/z=476 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809376B2
Source datasetuspto-grants-2014_08
ORD IDord-b9fd042f2e1344769c2263ca64405503
Source noteuspto-grants-2014_08