HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365531Generated: October 31, 2026
Water → tert-butyl N-[1-(aminomethyl)cyclopentyl]carbamate
https://huagongshe.com/reaction/2365531
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | tert-butyl N-(1-cyanocyclopentyl)carbamate | HCID 16740508 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl N-[1-(aminomethyl)cyclopentyl]carbamate | HCID 16740809 | — |
Reaction Steps
To a cooled 0° C. solution of (1-cyano-cyclopentyl)-carbamic acid tert-butyl ester (430 mg, 2.04 mmol) in dry THF (4.3 ml) under an atmosphere of argon is added dropwise 1.0 M LiAlH4 (6.13 ml, 6.13 mmol). The reaction mixture is allowed to warm to room temperature and stirred for 3.5 hours. The mixture is then re-cooled to 0° C. and cautiously quenched with water (0.4 ml): 15% NaOH (0.8 ml): water (1.2 ml) (1:2:3 eq). The resultant mixture is filtered through Celite® (filter material) to remove the inorganic solids and rinsed with MeOH. The filtrate is concentrated in vacuo, to yield a white solid, which is purified by chromatography on silica eluting with 30% MeOH in DCM to afford (1-Aminomethyl-cyclopentyl)-carbamic acid tert-butyl ester; [M+H]+ 215.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08697687B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e284a884a8f140498aa6fde4c8306f56 |
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| Source note | uspto-grants-2014_04 |
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