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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037375Generated: October 30, 2026

Chloroacetyl chloride → 7-Iodo-6-phenyl-1H-4,5-dioxa-1-aza-phenanthrene-2,8-dione

https://huagongshe.com/reaction/1037375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Amino-8-hydroxy-3-iodo-2-phenyl-chromen-4-oneHCID 67067919—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventChloroformHCID 6212—
Product7-Iodo-6-phenyl-1H-4,5-dioxa-1-aza-phenanthrene-2,8-dioneHCID 6706782799.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 7-amino-8-hydroxy-3-iodo-2-phenyl-chromen-4-one (150 mg, 0.40 mmol), benzyltriethylammonium chloride (91 mg, 0.40 mmol) and NaHCO3 (168 mg, 2 mmol) in CHCl3 (5 mL) at 0° C. was added a solution of chloroacetyl chloride (35 μL, 0.44 mmol) in CHCl3 (1 mL) dropwise over 30 mins. The reaction mixture was stirred at 0° C. for 2 hours before heating at 50° C. for 18 hours. The resultant mixture was cooled to RT and was partitioned between DCM and water. The aqueous phase was filtered and the solid collected and azeotroped with methanol to give the title compound as a beige solid (167 mg, 99%). LCMS (Method G): RT=3.18 min, [M+H]+=420.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546376B2
Source datasetuspto-grants-2013_10
ORD IDord-22c131d6879c4537a5ed3bd74d568b7b
Source noteuspto-grants-2013_10