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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387346Generated: October 30, 2026

Hydrochloric Acid → 4-Bromo-2-(cyclopropylmethyl)thiophene

https://huagongshe.com/reaction/387346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(4-Bromothiophen-2-yl)(cyclopropyl)methanoneHCID 59332599—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
Product4-Bromo-2-(cyclopropylmethyl)thiopheneHCID 59332713—

Reaction Conditions

Temperature160 °C

Reaction Steps

(4-bromo-2-thienyl)(cyclopropyl)methanone (1.02 g, 4.4 mmol) was diluted in ethylene glycol (3.75 mL). Potassium hydroxide (809 mg, 14.4 mmol, 3.3 eq) and hydrazine hydrate (0.58 mL, 18 mmol, 4.2 eq) were added, and the reaction mixture was heated at 160° C. for 45 minutes behind a blast shield. The reaction was cooled to room temperature, water was added, and the pH adjusted to acidic (by pH paper) with 6M aqueous HCl. The mixture was extracted with dichloromethane, the combined organics dried over sodium sulfate, filtered, and concentrated. The crude product was purified by isco combiflash, eluting with 0-10% ethyl acetate in hexanes. The title compound was obtained as clear colorless oil (50 mg, 5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372875B2
Source datasetuspto-grants-2013_02
ORD IDord-366ee0119e0f49d7b0457377c39b5e6c
Source noteuspto-grants-2013_02