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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526426Generated: November 3, 2026

Water → (R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid zinc salt

https://huagongshe.com/reaction/1526426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acidHCID 53362086—
ReactantHCID 178476751HCID 178476751—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid zinc saltHCID 87389269—

Reaction Conditions

Temperature60 °C

Reaction Steps

(R)-2-(9-Chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid [15 mg] was dissolved in THF [0.5 mL] and heated to 60° C. Aqueous Zn(OAc)2 [8.0 uL, 1.95 M] was added and the reaction mixture was cooled to 35° C. over 24 h. Water [8 uL] was added and the mixture was stirred at room temperature for 24 h. The reaction mixture was concentrated to dryness and EtOAc was added to provide a white solid which was collected by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085581B2
Source datasetuspto-grants-2015_07
ORD IDord-b365c1797b344cbfacf576fe8c24f9b9
Source noteuspto-grants-2015_07