HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750504Generated: October 31, 2026
Naphthalene → tert-Butyl N-(2-amino-1-methylcyclopentyl)carbamate
https://huagongshe.com/reaction/1750504
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | tert-butyl N-[1-methyl-2-(4-methylbenzenesulfonamido)cyclopentyl]carbamate | HCID 118024589 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | tert-Butyl N-(2-amino-1-methylcyclopentyl)carbamate | HCID 84783510 | — |
Reaction Steps
A mixture of lithium granules (7.17 g, 1195 mmol) and naphthalene (57.39 g, 448.36 mmol) in dry dimethoxyethane (1900 ml) was stirred at room temperature for 2 hours. The deep blue solution was then cooled to 0° C. and a solution of tert-butyl N-[1-methyl-2-(4-methylbenzenesulfonamido)cyclopentyl]carbamate (55.0 g, 149.45 mmol) in dry dimethoxyethane (300 ml) was added drop wise over 30 minutes. The mixture was stirred at 0° C. for 3 hours. The un-dissolved lithium was removed by filtration and 1M HCl solution (aq, 720 ml) was added to the filtrate. The organic layer was washed with further 1M HCl (aq, 2×600 ml). The combined aqueous layers were washed with diethyl ether (2×600), and then basified with 2M NaOH (aq) to give pH 12-14. The aqueous layer was then extracted with ethyl acetate (5×600 ml). The combined organics were dried over sodium sulfate and then concentrated in vacuo. This was then purified by column chromatography (silica, 0-4% methanol/DCM) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156829B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-8fbc0323bf7f4380af944681acead54b |
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| Source note | uspto-grants-2015_10 |
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