HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255470Generated: November 2, 2026
Hydrazine hydrate (1:1) → HCID 178514433, compound
https://huagongshe.com/reaction/1255470
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 178501260 | HCID 178501260 | — |
| Product | HCID 178514433 | HCID 178514433 | 86% |
Reaction Steps
A mixture of trans-4-(3-chloro-phenoxy)-cyclohexanecarboxylic acid methyl ester (0.25 g, 0.93 mmol) and hydrazine hydrate (0.044 ml, 0.91 mmol) was heated at 120° C. for 22 h. Addition of further hydrazine hydrate (0.020 ml, 0.42 mmol) was followed by stirring at 120° C. for 5 h. After cooling to room temperature the reaction mixture was partitioned between ethyl acetate (50 ml) and 1 M aqueous sodium hydroxide solution (50 ml). The layers were separated and the aqueous layer was extracted with a 50-ml portion of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (0.21 g, 86%) as white solid, which was used in the next step without further purification. MS m/e: 269 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461152B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-53c47a1f56dd4badbebca787504c6bc2 |
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| Source note | uspto-grants-2013_06 |
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