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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728128Generated: November 1, 2026

Acetyl chloride → HCID 76568078, compound

https://huagongshe.com/reaction/1728128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHexamethyldisilazaneHCID 13838—
Reactant2-Fluoro-5-iodobenzaldehydeHCID 16217058—
ReactantHCID 57565907HCID 57565907—
ReactantButyllithiumHCID 178418339—
ProductHCID 76568078HCID 76568078—

Reaction Steps

In a manner similar to the method described in example 190b, 2-fluoro-5-iodobenzaldehyde (2.62 g, 10.5 mmol) (Aldrich) 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 (2.14 mL, 10.5 mmol), n-butyllithium (2.5 M, 4.2 mL, 10.5 mmol), trimethylsilyl chloride (1.33 mL, 10.5 mmol), triethylamine (1.9 mL, 13.6 mmol) and acetyl chloride (0.97 mL, 13.6 mmol) to give crude 1-(2-fluoro-5-iodophenyl)-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-5269cd9532314a57833d45a8207f69b4
Source noteuspto-grants-2009_02