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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399225Generated: October 31, 2026

Oxalyl chloride → HCID 18703878, compound

https://huagongshe.com/reaction/399225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 21714793HCID 21714793—
SolventDimethylformamideHCID 6228—
ProductHCID 18703878HCID 1870387894%

Reaction Conditions

Temperature0 °C

Reaction Steps

To ice-cold DMF (1 ml) under an argon atmosphere was added oxalyl chloride (68 ml, 0.78 mmol). After stirring for 5 min at 0° C., a solution of (1RS,2SR,3SR)-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carboxamide (150 mg, 0.39 mmol) in DMF (2 ml) was added, and stirring was continued for an additional 10 min at 0° C. The reaction mixture was partitioned between EtOAc and 3M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with H2O, aqueous NaHCO3, H2O and saturated aqueous NaCl and dried. The solvent was removed in vacuo to afford the title compound as a white solid (135 mg, 94%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817693
Source datasetuspto-grants-1998_10
ORD IDord-082f7c72b94d464a8347e1874c19a277
Source noteuspto-grants-1998_10