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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657716Generated: November 2, 2026

Triethylamine → 1-Boc-3-Phenyl-pyrrolidine

https://huagongshe.com/reaction/657716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(3R,4S)-3-formyl-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 58981949—
Solvent1,2-DichloroethaneHCID 11—
Product1-Boc-3-Phenyl-pyrrolidineHCID 1123038880.9%

Reaction Steps

To a solution of 3-(4-methanesulfonylbenzyl)-bicyclo[3.2.1]-1α,3,8-triaza-spiro[4.5]dodecan-2,4-dione hydrochloride (40 mg, 0.1 mmol) in 1.7 mL of anhydrous DCE were added successively 28 mg (0.1 mmol) of (3R,4S)-3-formyl-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl ester and 17 μL (0.12 mmol) of triethylamine. The reaction mixture was agitated at room temperature for 10 minutes before adding 26 mg (0.125 mmol) of sodium triacetoxyborohydride. After an overnight agitation, 2 mL of saturated solution of sodium bicarbonate was added. The solution was then extracted with DCM (2×2 mL), dried over sodium sulfate, filtered and concentrated in vacuo. The crude mixture was purified by bond elute (ethyl acetate to 5% methanol/DCM) to yield (3S,4S)-3-[3-(4-methanesulfonylbenzyl)-bicyclo[3.2.1]-2,4-dioxo-1α,3,8-triaza-spiro[4.5]dodec-8-ylmethyl]-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a white solid (20 mg, 32.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076349B2
Source datasetuspto-grants-2011_12
ORD IDord-d009517039a746bdb7cbdc79fdafd0b9
Source noteuspto-grants-2011_12