HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192903Generated: November 1, 2026
Potassium Hydroxide → [3-Bromo-4-(cyclopropylsulfanyl)phenyl]acetic acid
https://huagongshe.com/reaction/2192903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 59571040 | HCID 59571040 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | [3-Bromo-4-(cyclopropylsulfanyl)phenyl]acetic acid | HCID 59570913 | 94.4% |
Reaction Steps
To hydrazine monohydrate (16.9 mL) was added [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetic acid (15 g) under ice-cooling, followed by stirring at 80° C. for 10 minutes. To the reaction mixture was added potassium hydroxide (8.22 g), followed by stirring at 80° C. for 20 minutes and then stirring at 100° C. overnight. After leaving it to be cooled at room temperature, concentrated hydrochloric acid (50 mL) was added thereto under ice-cooling, followed by extraction with chloroform (50 mL×3). The organic layer was sequentially washed with 1 M hydrochloric acid (50 mL×2) and saturated brine (50 mL), and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure to obtain [3-bromo-4-(cyclopropylsulfanyl)phenyl]acetic acid (13.5 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329707B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-72975d8db82f45dab6909ee6b92eb0e1 |
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| Source note | uspto-grants-2012_12 |
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