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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7-Amino-8-hydroxy-3-iodo-2-phenyl-chromen-4-one | HCID 67067919 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-Iodo-6-phenyl-1H-4,5-dioxa-1-aza-phenanthrene-2,8-dione | HCID 67067827 | 99.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546376B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-22c131d6879c4537a5ed3bd74d568b7b |
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| Source note | uspto-grants-2013_10 |
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