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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330820Generated: October 30, 2026

Diisopropylamine → HCID 2185393, compound

https://huagongshe.com/reaction/330820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl AcetateHCID 8857—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant1-Ethoxy-4-ethynylbenzeneHCID 2775124—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2185393HCID 2185393—

Reaction Steps

To 1.60 g (11.0 mmol) 4-ethoxyphenylacetylene in 40 mL THF are added 3.10 g (11.0 mmol) 1-bromo-4-iodo-benzene under argon, followed by 0.18 g (0.22 mmol) Pd(dppf)Cl2CH2Cl2 as catalyst, 0.04 g (0.22 mmol) copper(I)iodide and 3.10 mL (21.9 mmol) diisopropylamine as base. The mixture is stirred at rt for 3 h. After that time, EtOAc is added and the organic layer is washed with ammonia (5%, 2×) and water (1×). The organic layer is separated, dried over magnesium sulphate and the solvent is evaporated. The residue is purified by column chromatography (silicia gel; PE:EtOAc 9:1) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877754B2
Source datasetuspto-grants-2014_11
ORD IDord-e5a57b4e3971496cb2b74432d00a128d
Source noteuspto-grants-2014_11