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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45434Generated: October 30, 2026

Water → HCID 178489288, compound

https://huagongshe.com/reaction/45434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-BromoanisoleHCID 11358—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178422466HCID 178422466—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418851HCID 178418851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178489288HCID 17848928826%

Reaction Conditions

Temperature-100 °C

Reaction Steps

To a solution of 2.25 g (5.0 mmol) of 34 in 20 mL of THF, 4.0 mL (10.0 mmol) of 2.5 M nBuLi in hexanes was added at −80° C. This mixture was stirred for 1 hr, then cooled to −100° C. and 10.8 mL (10.8 mmol) of 1.0 M ZnCl2 in THF was added. The resulting mixture was slowly warmed to ambient temperature, stirred for 30 min, and then 2.82 g (15.0 mmol) of 2-bromoanisole and 0.14 g (0.25 mmol) of Pd(PtBu3)2 was added. This mixture was refluxed for 8 hr, then 5 mL of water was added. The resulting mixture was passed through a short layer of silica gel 60. The silica gel layer was additionally washed with 30 mL of dichloromethane. The combined organic elute was evaporated to dryness. The product was isolated by flash chromatography on silica gel 60 (40-63 um, eluent: from hexanes to hexanes-diethyl ether, 20:1, vol.) to give 0.55 g (26%) of a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541521B2
Source datasetuspto-grants-2013_09
ORD IDord-ba38f7d4036a42b983404df945cc5402
Source noteuspto-grants-2013_09