HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969638Generated: November 1, 2026
Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate → 4-(Dibenzylamino)-2-methylcyclopentanecarboxylic acid
https://huagongshe.com/reaction/1969638
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate | HCID 58010318 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(Dibenzylamino)-2-methylcyclopentanecarboxylic acid | HCID 58557535 | 98.3% |
Reaction Steps
Ethyl 4-(dibenzylamino)-2-methylcyclopentanecarboxylate (3.65 g, 10.38 mmol) was dissolved in a mixture of HC; (6 N aqueous, 20 mL) and 1,4-dioxane (50 mL) and the resulting mixture was heated at about 60° C. for about 72 h. The organic solvent was removed under reduced pressure. The aqueous phase was neutralized by the addition of saturated aqueous NaHCO3 (40 mL) and extracted with EtOAc (50 mL). The organic phase was washed with brine (40 mL), dried over anhydrous MgSO4 and coned under reduced pressure to yield 4-(dibenzylamino)-2-methylcyclopentanecarboxylic acid (3.3 g, 98%) as a white amorphous solid: LC/MS (Table 1, Method a) Rt=1.66 min.; MS m/z 324 (M+H)+. The procedure in Step A, Preparation #33 was utilized to provide (1S,2R,4S)-4-(dibenzylamino)-2-methylcyclopentanecarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426411B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c6e497233efa4ecc9aa642349d79a46a |
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| Source note | uspto-grants-2013_04 |
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