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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095142Generated: October 30, 2026

Acetyl chloride → 1-[5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene

https://huagongshe.com/reaction/1095142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHexamethyldisilazaneHCID 13838—
Reactant4-(2-Formyl-4-iodo-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57743163—
Reactant5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-benzaldehydeHCID 57743296—
ReactantButyllithiumHCID 178418339—
Product1-[5-Chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadieneHCID 66641536—

Reaction Steps

In a manner similar to the method described in example 1d, 5-chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-benzaldehyde (1.5 g, 5 mmol) was used as the starting material in place of 4-(2-formyl-4-iodo-phenoxymethyl)-piperidine-1-carboxylic acid tert-butyl ester to react with 1,1,3,3,3-hexamethyldisilazane (0.8 g, 5 mmol), n-butyllithium (2.5 M, 2 mL, 5 mmol), trimethylsilyl chloride (0.55 g, 5 mmol), triethylamine (0.7 g, 6.8 mmol) and acetyl chloride (0.5 g, 6.8 mmol) to give crude 1-[5-chloro-2-(1,4-dioxa-spiro[4.5]dec-8-yloxy)-phenyl]-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 numberUS08134001B2
Source datasetuspto-grants-2012_03
ORD IDord-6d3b335b08c14016b052ccabd28f1b99
Source noteuspto-grants-2012_03