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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040432Generated: October 30, 2026

Iodine → HCID 57517766, compound

https://huagongshe.com/reaction/2040432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-3-methylthiopheneHCID 84314—
Reactant5-chloro-1H-indole-2,3-dioneHCID 87203—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57517766HCID 5751776688.5%

Reaction Conditions

Temperature21 °C

Reaction Steps

Magnesium turnings (6.8 g, 0.27 mmol) are introduced into diethyl ether (30 ml), and, while stirring, a solution of 2-bromo-3-methyl-thiophene (50 g, 0.282 mol) in diethyl ether (100 ml) is added dropwise. The reaction can be initiated if necessary by adding iodine crystals. During the addition, the reaction mixture should boil gently. After the addition, the mixture was stirred at room temperature for 1 hour. A suspension of 5-chloroisatin (19 g, 0.105 mol) in THF (200 ml) was added to the Grignard solution while cooling slightly (temperature 18-24° C.) and the mixture was stirred at room temperature for 30 min. The reaction mixture was stirred into ammonium chloride solution and extracted several times with ethyl acetate. The combined organic phases were washed with saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was stirred with diethyl ether. The resulting precipitate was filtered off, washed with diethyl ether and dried. 26 g of the desired intermediate were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580842B2
Source datasetuspto-grants-2013_11
ORD IDord-7187006336ae4beeb8bfb5503771a25f
Source noteuspto-grants-2013_11