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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751850Generated: October 27, 2026

Diethyl Ether → HCID 59678633, compound

https://huagongshe.com/reaction/1751850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantHCID 59678679HCID 59678679—
ReactantHCID 59678709HCID 59678709—
ReactantButyllithiumHCID 178418339—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59678633HCID 59678633—

Reaction Steps

To a solution of 4-but-2-ynyloxy-1,2-dimethoxybenzene (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-8-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-8-nitro-2H-chromen-6-yl)-but-2-yn-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09161997B2
Source datasetuspto-grants-2015_10
ORD IDord-9c534571fdc14ec9a5922ed16363b9f7
Source noteuspto-grants-2015_10