HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066911Generated: November 1, 2026
Trifluoroacetic acid → (trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1066911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine | HCID 353442 | — |
| Reactant | Ethyl 5-methylhex-2-enoate | HCID 6436900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl ester | HCID 69861599 | 44.2% |
Reaction Steps
N-Benzyl-N-(methoxymethyl)trimethylsilylmethylamine (2.84 g, 12 mmol), followed by TFA (1.0 M solution in CH2Cl2, 1.0 mL, 1 mmol) were added to a solution of (E)-5-methyl-hex-2-enoic acid ethyl ester (1.56 g, 10.0 mmol) in methylene chloride (30 mL) maintained at −5° C. under nitrogen atmosphere. After 15 minutes, the bath was removed and stirring was continued overnight. Saturated sodium bicarbonate was added, and the organic portion was separated, washed with brine, and dried. The product was purified by chromatography on silica gel, and compound was eluted with 20% ethyl acetate in hexane to give (trans)-1-Benzyl-4-isobutyl-pyrrolidine-3-carboxylic acid ethyl ester 3 as an oil (1.28 g, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245801B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-264feddedee446da9f1f356b42220804 |
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| Source note | uspto-grants-2001_06 |
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