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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410620Generated: October 31, 2026

Benzoyl chloride → HCID 68966117, compound

https://huagongshe.com/reaction/2410620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 178520590HCID 178520590—
SolventPyridineHCID 1049—
ProductHCID 68966117HCID 6896611765%

Reaction Steps

In a 100 mL two-neck flask under a static head of nitrogen 12-bromo-dodecanol (5.0 g, 18.9 mmol) is weighed, pyridine (25 mL) is added and the whole is brought to 0° C. with an external bath of ice and salt. Benzoyl chloride is dripped slowly and, when adding is finished, the ice bath is removed and the whole is left stirring at room temperature. After 18 hours ethyl acetate (100 mL) and distilled water (100 mL) are added. The organic phase is washed 3 times with distilled water (3×50 mL) and anhydrified on anhydrous sodium sulphate. It is filtered under a vacuum and the solvent is eliminated in the Rotovapor and in the high vacuum pump. The product is purified with column chromatography on silica gel with an eluant mixture of petroleum ether/ethylic ether 5/1. 4.5 g of 12-bromododecyl benzoate are isolated as a colourless oil with a yield of 65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816107B2
Source datasetuspto-grants-2014_08
ORD IDord-297b26d7ea33448f8e313ef58d8e4a61
Source noteuspto-grants-2014_08