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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516076Generated: November 5, 2026

Diethyl Ether → HCID 59678602, compound

https://huagongshe.com/reaction/1516076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 59678695HCID 59678695—
ReactantHCID 59678709HCID 59678709—
ReactantButyllithiumHCID 178418339—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59678602HCID 59678602—

Reaction Steps

To a solution of 4-but-2-ynyloxy-1,2-dimethoxy-benzene (1.66 g, 8.66 mmol) in THF (75 mL) is added n-butyl lithium (5.54 ml of 1.6 M solution in THF, 8.86 mmol) at −78° C. After 30 min., 5-methoxy-2,2-dimethyl-7-nitro-2H-chromene-6-carbaldehyde (2.17 g, 8.25 mmol) in THF (50 mL) is added. The reaction is stirred for 1 h and then quenched with sat. NH4Cl and extracted with ethyl acetate. The combined organic layers are washed with brine and dried over Na2SO4. The resulting crude material is dissolved in dichloromethane (20 mL) and MnO2 (5.3 g, 61 mmol) is added. After the reaction is stirred overnight at room temperature, ether is added and the suspension is filtered through a pad of celite and silica gel to afford 4-(3,4-dimethoxy-phenyoxy)-1-(5-methoxy-2,2-dimethyl-7-nitro-2H-chromen-6-yl)-but-2-yn-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08226929B2
Source datasetuspto-grants-2012_07
ORD IDord-041771b8101f43d3b6c8e1b33532fa4e
Source noteuspto-grants-2012_07