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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186743Generated: October 31, 2026

Oxalyl chloride → HCID 86690015, compound

https://huagongshe.com/reaction/1186743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86690016HCID 86690016—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86690015HCID 86690015—

Reaction Steps

To an anhydrous tetrahydrofuran (5 mL) solution of oxalyl chloride (0.12 mL) was added dropwise an anhydrous tetrahydrofuran (10 mL) solution of N2-(4-methoxyphenyl)naphthalene-1,2-diamine (322 mg, 1.22 mmol) under cooling in an ice-bat. The mixture was stirred under cooling in ice-bath for 30 minutes and at room temperature for one hour. The reaction mixture was poured into a saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure. The obtained solid was filtered. The crude crystal was washed with ethyl acetate and hexane to obtain the titled compound as a slightly off-white crystal (220 mg, yield 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673915B2
Source datasetuspto-grants-2014_03
ORD IDord-d7c502255c6849c9a09d8e4c3f74ae3f
Source noteuspto-grants-2014_03