HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921666Generated: October 26, 2026
N-Methylcyclohexylamine → N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester
https://huagongshe.com/reaction/1921666
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester | HCID 67493517 | 90.1% |
Reaction Steps
10 g of 4-bromobutyric acid ethyl ester and 15 g of N-cyclohexyl-N-methylamine were added to 40 mL of ethanol, and the mixture was heated to reflux for 2 hours. After air-cooling, the mixture was concentrated under reduced pressure and extracted with 200 mL of ethyl acetate. The extracted material was washed with purified water, dried with magnesium sulfate, and then concentrated. The obtained residue was distilled under reduced pressure to give 10.5 g of N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester. The obtained N-cyclohexyl-N-methyl-gamma-aminobutyric acid ethyl ester was added to a sodium hydroxide solution (2.4 g of sodium hydroxide/100 mL of purified water), and THF was added thereto until the mixture became homogeneous. After stirring at room temperature for 3 hours, the mixture was neutralized with DOWEX50W [H+ form] and concentrated under reduced pressure. The obtained residue was recrystallized to give 5.2 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173705B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-c25ed5548a08491982eb43d32fab1c60 |
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| Source note | uspto-grants-2012_05 |
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