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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195823Generated: November 2, 2026

Oxalyl chloride → HCID 15712740, compound

https://huagongshe.com/reaction/1195823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 15712739HCID 15712739—
ProductHCID 15712740HCID 15712740—

Reaction Steps

Oxalyl chloride (10 ml) was added to 2-isopropyl-7-(p-nitrophenyl)heptanoic acid (200 mg; prepared in reference example 6). The solution was stirred for 10 mins, and concentrated to dryness. Methylene chloride (10 ml) was added to this residue followed by the addition of 2-hydroxymethylpyrrolidine (0.087 ml). The solution was cooled with ice. Triethylamine (0.143 ml) was added to this reaction solution. The solution was stirred for 30 mins. Subsequently, the reaction solution was evaporated. The residue was purified by column chromatography on silica gel to give the title compound (150 mg) having the following physical data:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112847
Source datasetuspto-grants-1992_05
ORD IDord-ee6ad56ff7054d8da338db03bedc62c6
Source noteuspto-grants-1992_05