HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750513Generated: October 30, 2026
Lithium Hydroxide → 2-[(tert-Butoxycarbonyl)amino]-2-methylcyclopentane-1-carboxylic acid
https://huagongshe.com/reaction/1750513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 2-{[(tert-butoxy)carbonyl]amino}-2-methylcyclopentane-1-carboxylate | HCID 118308259 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(tert-Butoxycarbonyl)amino]-2-methylcyclopentane-1-carboxylic acid | HCID 53396825 | — |
Reaction Steps
Lithium hydroxide (23.50 g, 981 mmol) was added to a solution of methyl 2-{ [(tert-butoxy)carbonyl]amino}-2-methylcyclopentane-1-carboxylate (50.51 g, 196 mmol) in THF (300 ml) and water (150 ml). The reaction was heated at 50° C. for 18 hours and then to 60° C. for 18 hours. The reaction was concentrated in vacuo and then acidified to pH 7 with concentrated HCl and then to pH 3 with 2 M HCl (aq). The organics were extracted with ethyl acetate (3×300 ml) and the combined organics were washed with brine (50 ml), dried over magnesium sulfate and concentrated in vacuo to afford the title compound which was used without further purification.
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-e64c5a1d17e94237be851bde0221560c |
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| Source note | uspto-grants-2015_10 |
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