ChemicalBook--->CAS DataBase List--->20780-75-0

20780-75-0

20780-75-0 Structure

20780-75-0 Structure
IdentificationBack Directory
[Name]

BUTTPARK 148\07-01
[CAS]

20780-75-0
[Synonyms]

4-Iodoisatin
BUTTPARK 148\07-01
4-iodoindoline-2,3-dione
4-IODO-1H-INDOLE-2,3-DIONE
1H-Indole-2,3-dione, 4-iodo-
4-iodo-2,3-dihydro-1H-indole-2,3-dione
[Molecular Formula]

C8H4INO2
[MDL Number]

MFCD03427300
[MOL File]

20780-75-0.mol
[Molecular Weight]

273.03
Chemical PropertiesBack Directory
[Melting point ]

227-229°
[density ]

2.106±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

8.88±0.20(Predicted)
[Appearance]

Brown to orange Solid
Questions And AnswerBack Directory
[Uses]

4-Iodine indigo is a heterocyclic organic compound that can be used as a pharmaceutical synthesis intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

BUTTPARK 148\07-01(20780-75-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

(2E)-2-(hydroxyimino)-N-(3-iodophenyl)acetamide

63608-68-4

BUTTPARK 148\07-01

20780-75-0

General procedure for the synthesis of 4-iodoindoline-2,3-dione from 2-(N-hydroxyimino)-N-(3-iodophenyl)acetamide: Sulfuric acid (1L) was placed in a 3L beaker on a hot plate, heated to 60°C and removed from the heat source. Compound 8a was added in batches over a period of 30 minutes under continuous stirring, controlling the reaction temperature to not exceed 65 °C. Subsequently, the reaction mixture was heated to 80 °C and maintained for 15 min, after which it was cooled to 70 °C and placed in an ice bath for further cooling. The reaction solution was slowly decanted into crushed ice (5 L) and allowed to stand for 1 h. The orange-red precipitate was collected by filtration. The product was washed with deionized water (400 mL) with stirring and filtered again to give a mixture of compound 8b with 6-iododihydroindole-2,3-dione. The crude product was dissolved in a solution of deionized water (200 mL) containing sodium hydroxide (20 g) and heated to 60 °C to dissolve it completely, followed by adjusting the pH with acetic acid to 4.9. After standing for 0.5 h and cooling to 35 °C, the precipitate of compound 8b precipitated was filtered and washed with deionized water (50 mL) to give the final product (38.37 g, 59% yield). Mass spectrometry analysis showed [M+H]+ m/z 274.

[References]

[1] Patent: WO2017/211303, 2017, A1. Location in patent: Page/Page column 40
[2] European Journal of Medicinal Chemistry, 2018, vol. 145, p. 370 - 378
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