HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1685317Generated: November 3, 2026
1-Phenylcyclopropanecarboxamide → 1-Phenylcyclopropanemethanamine
https://huagongshe.com/reaction/1685317
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenylcyclopropanecarboxamide | HCID 292217 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenylcyclopropanemethanamine | HCID 70287 | 49% |
Reaction Steps
A solution of 1-phenylcyclopropanecarboxamide (0.450 g, 2.79 mmol) in tetrahydrofuran (5 mL) was slowly added to a suspension of LAH (0.117 g, 3.07 mmol) in tetrahydrofuran (5 mL) at 23° C. over 2 minutes. The reaction was then heated to 65° C. for 6 hours. The reaction was quenched with the Rochelle salt (1N in water, 10 mL) and extracted with ethyl acetate (3×). The combined organic layers were then dried over anhydrous magnesium sulfate, filtered and concentrated to give the crude title material (0.200 g, 49%) as an oil which was used as such in the next reaction. An aliquot was purified on preparative HPLC (ammonium acetate/water/acetonitrile). 1H NMR (400 MHz, CDCl3, acetic acid salt) δ: 0.83-0.94 (4H, m), 1.98 (3H, s), 2.90 (2H, s), 4.98 (3H, br s), 7.23-7.37 (5H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148400B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-fab299aae0f546779a72abe5a7e82cf8 |
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| Source note | uspto-grants-2012_04 |
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