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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764144Generated: November 3, 2026

Oxalyl chloride → HCID 54077320, compound

https://huagongshe.com/reaction/1764144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodiumHCID 5360545—
ReactantHCID 20306750HCID 20306750—
SolventBenzeneHCID 241—
ProductHCID 54077320HCID 54077320—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of 12 g of the sodium salt of α-[p-(1-cyclohexenyl)-phenoxy]-heptanoic acid in 200 ml of absolute benzene are added with stirring at 5°C 25 g of oxalyl chloride. The mixture is continuously stirred overnight at room temperature, then evaporated to dryness in vacuo. The residue is dissolved in 200 ml of absolute benzene are added with stirring at 5° C 25 g of oxalyl chloride. The mixture is continuously stirred overnight at room temperature, then evaporated to dryness in vacuo. The residue is dissolved in 200 ml of absolute benzene and filtered under anhydrous conditions. The filtrate is evaporated to dryness in vacuo. The residue yields the crude α-[p-(1-cyclohexenyl)-phenoxy]-heptanoic acid chloride, which is used directly for further processing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115416
Source datasetuspto-grants-1978_09
ORD IDord-3745bfcdabf3485494af5539dd306de8
Source noteuspto-grants-1978_09