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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453883Generated: October 29, 2026

Iodine → HCID 57831240, compound

https://huagongshe.com/reaction/453883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant2-BromothiopheneHCID 13851—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1,1-Dimethylethyl 4-cyano-4-(dimethylamino)-1-piperidinecarboxylateHCID 57504797—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 57831240HCID 5783124064.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A little iodine was added to a mixture of 5.6 g (3 eq.) magnesium and 20 ml dry diethyl ether, followed over a period of 10 min by 5 g 2-bromothiophene, and the mixture was stirred for a further 10 min. Once the reaction had started, 33.5 g (2.6 eq.) 2-bromothiophene dissolved in 80 ml diethyl ether were added dropwise and the mixture was stirred for a period of 2 h at room temperature. The Grignard reagent prepared in the preceding step was added dropwise to a solution of 20 g (1 eq.) tert-butyloxycarbonyl-4-cyano-4-(dimethylamino)piperidine dissolved in 200 ml THF and stirred overnight at room temperature. The reaction course was monitored by thin-layer chromatography (50% EtOAc/hexane). Once the conversion was complete, the reaction solution was cooled to 0° C., mixed with saturated NH4Cl solution, extracted with ethyl acetate (3×100 ml) and the combined organic phases were dried with Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (alox neutral; 30% EtOAc/hexane). 6.1 g (25%) of product were obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-a696a281ff7e451c9008e6cea32d7a03
Source noteuspto-grants-2013_07