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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731166Generated: November 2, 2026

Oxalyl chloride → HCID 21495612, compound

https://huagongshe.com/reaction/1731166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15727607HCID 15727607—
ProductHCID 21495612HCID 21495612—

Reaction Steps

Using the procedure of Step A of Example II, 22.98 g of 3-(m-benzoyl-phenyl)-propionic acid and 115 ml of oxalyl chloride were reacted to obtain 24.59 g of 3-(m-benzoyl phenyl)-propionyl chloride. A solution of the said acid chloride in 50 ml of anhydrous ether was added with stirring at 25° C in 45 minutes to 1,460 ml an ether solution of 10.5 g/liter of diazomethane and the mixture was stirred at 25° C for 16 hours and then evaporated to dryness under reduced pressure to obtain 29 g of raw product which was purified by chromatography over silica with a 95-5 methylene chloride-ethyl acetate eluant which was evaporated to dryness to obtain 19 g of 3-(4'-diazo-3'-oxo-pentyl)-benzophenone. STEP B: 2,3-isopropylidenedioxypropyl 4-(m-benzoyl-phenyl)-2-methyl-butyrate

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03995056
Source datasetuspto-grants-1976_11
ORD IDord-3a001db3bb6141479b6e0a8d110ef8f2
Source noteuspto-grants-1976_11