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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362145Generated: November 1, 2026

Triethylamine → Methyl 4-amino-2-chloro-5-((trimethylsilyl)ethynyl)benzoate

https://huagongshe.com/reaction/2362145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantBenzoic acid, 4-amino-2-chloro-5-iodo-, methyl esterHCID 11839203—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-amino-2-chloro-5-((trimethylsilyl)ethynyl)benzoateHCID 59625799—

Reaction Steps

To a mixture of compound 70n (0.642 mmol, 200 mg), Cut (0.064 mmol, 12.2 mg) and Pd(PPh3)2Cl2 (0.064 mmol, 45 mg) in THF (2 mL) was added ethynyltrimethylsilane (0.963 mmol, 95 mg) followed by Et3N (7.19 mmol, 1 mL) under N2. The reaction mixture was stirred at room temperature for 1.5 h and then partitioned between EtOAc and water. The organic layer was concentrated and purified by flash column chromatography (silica gel, 15% EtOAc/hexanes) to give compound 70p.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691805B2
Source datasetuspto-grants-2014_04
ORD IDord-619f4891bcb34fbfb1d64fe5642a89ce
Source noteuspto-grants-2014_04