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

HRID 387346Notes

Reaction equation

HRID 387346 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:7]([CH:9]2[CH2:11][CH2:10]2)=O)[S:5][CH:6]=1.[OH-].[K+].O.NN.Cl>C(O)CO.O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][CH:9]2[CH2:11][CH2:10]2)[S:5][CH:6]=1

Participants

7

Conditions

Temperature
160 °C

Procedure

(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%).

Workup

  1. temperatureThe reaction was cooled to room temperature
  2. extractionThe mixture was extracted with dichloromethane
  3. dry with materialthe combined organics dried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was purified by isco combiflash
  7. washeluting with 0-10% ethyl acetate in hexanes

Sources & evidence

ORD record
ord-366ee0119e0f49d7b0457377c39b5e6c
Source dataset
uspto-grants-2013_02
Patent number
US08372875B2

Reaction notes

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