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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728142Generated: October 30, 2026

Acetyl chloride → HCID 76568111, compound

https://huagongshe.com/reaction/1728142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHexamethyldisilazaneHCID 13838—
Reactant1-Benzofuran-5-carbaldehydeHCID 2773875—
ReactantHCID 57565907HCID 57565907—
ReactantButyllithiumHCID 178418339—
ProductHCID 76568111HCID 76568111—

Reaction Steps

In a manner similar to the method described in example 190b, 1-benzofuran-5-carbaldehyde (1.2 g, 10 mmol) (Maybr-INT) was used as the starting material in place of 2-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-5-iodo-benzaldehyde to react with 1,1,3,3,3-hexamethyldisilazane (1.6 g, 10 mmol), n-butyllithium (2.5 M, 4 mL, 10 mmol), trimethylsilyl chloride (1.1 g, 10 mmol), triethylamine (1.36 g, 13.6 mmol) and acetyl chloride (1 g, 13.6 mmol) to give crude 1-(1-benzofuran-5-yl)-3-trimethylsilyoxy-2-aza-1,3-butadiene as a yellow gum and used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-df9eede6dca24d7e8436d9c3eadedab4
Source noteuspto-grants-2009_02