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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385710Generated: October 26, 2026

Hydrochloric Acid → 5-Bromo-3-(dichloromethyl)-2-nitrothiophene

https://huagongshe.com/reaction/385710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChloroformHCID 6212—
Reactant2-Bromo-5-nitrothiopheneHCID 83222—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-3-(dichloromethyl)-2-nitrothiopheneHCID 59525607—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 2-bromo-5-nitrothiophene (29 g, 139 mmol) and chloroform (12.37 mL, 153 mmol) in DMF (110 mL) was added dropwise to a solution of potassium tert-butoxide (62.6 g, 558 mmol) in THF (225 mL)/DMF (180 mL). The internal temperature was monitored and maintained at <−60° C. during the addition. Upon complete addition, the reaction was stirred at −78° C. for 30 minutes. 2 N HCl was added and the products were extracted into EtOAc (3×). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification of the residue by flash silica gel column chromatography (0-10% EtOAc-hexanes) gave the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-7fca4b71b7804915bee72842cc7079ce
Source noteuspto-grants-2013_02