HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698351Generated: November 1, 2026
1-Bromo-2-Chloroethane → 1-(Pyridin-4-yl)cyclopropanecarboxylic acid
https://huagongshe.com/reaction/1698351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-2-Chloroethane | HCID 7849 | — |
| Reactant | 4-Pyridineacetic acid | HCID 34228 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-(Pyridin-4-yl)cyclopropanecarboxylic acid | HCID 55267109 | — |
Reaction Steps
To a mixture of pyridin-4-yl-acetic acid (930 mg, 6.0 mmol) and 1-bromo-2-chloroethane (750 mg, 9.0 mmol) in 50% NaOH aq. solution (5 mL) is added benzyltriethylammonium chloride (680 mg, 3 mmol). The solution is heated to 60° C. and stirred at the temperature for 2 hours. After cooling down to rt, the aqueous layer is removed and the organic layer is neutralized with sat. NH4Cl aq. and extracted with Et2O. The combined organic phases are washed with H2O and dried over Na2SO4. Concentration under reduced pressure gives the title compound. The material is used in a next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163773B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-7b3c5e84698a4a1b92e141f58d7adfdd |
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| Source note | uspto-grants-2012_04 |
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