HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079378Generated: October 31, 2026
p-Fluorophenethylamine → HCID 57166725, compound
https://huagongshe.com/reaction/1079378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluorophenethylamine | HCID 4653 | — |
| Reactant | Cyclohexanemethanol | HCID 7507 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57166725 | HCID 57166725 | 59.7% |
Reaction Steps
A solution of 4.87 g (30 mmol) of carbonyldiimidazole and 3.43 g (30 mmol) of cyclohexylmethanol was stirred, under nitrogen and at room temperature, for 2-4 hours or the time until the TLC (silica gel; hexane-ethylacetate, 4:1) analysis indicated a complete disappearance of cyclohexylmethanol in the mixture. To this reaction mixture, a solution of 4-fluorophenylethyl amine (4.18 g, 30 mmol) in methylene chloride (5 mL) was added and stirred overnight. The TLC analysis indicated a complete disappearence of 4-fluorophenylethyl amine. The reaction mixture was extracted with 4×50 mL of methylene chloride. The combined extracts were washed with 5% HCl (2×50 mL),water, dried over MgSO4, and concentracted under vacuum. The solid was crystallized from hexane to furnish 5.0 g of N-(Cyclohexylmethyloxycarbonyl)-4-fluorophenylethyl amine (59% yield). mp 44°-45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05580878 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-c7283387541b4ecd9ba069e277de950b |
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| Source note | uspto-grants-1996_12 |
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