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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657717Generated: November 3, 2026

Sodium triacetoxyborohydride → 1-Boc-3-Phenyl-pyrrolidine

https://huagongshe.com/reaction/657717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(3R,4S)-3-formyl-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 58981949—
Solvent1,2-DichloroethaneHCID 11—
SolventDichloromethaneHCID 6344—
Product1-Boc-3-Phenyl-pyrrolidineHCID 11230388—

Reaction Steps

To 527 mg (2.22 mmol) of 1-isopropyl-3-methyl-bicyclo[3.2.1]-1β,3,8-triaza-spiro[4.5]dodecan-2-one in DCE (15 mL) was added 611 mg (2.22 mmol) of (3R,4S)-3-formyl-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl ester in DCE (10 mL) and stirred for 2 hours at room temperature. Sodium triacetoxyborohydride (706 mg, 3.33 mmol) was then added and the reaction mixture stirred overnight at room temperature. The reaction mixture was diluted with DCM, the organic layer washed with sodium bicarbonate, and then dried over sodium sulfate. The organic layer was concentrated and purified by flash silica gel chromatography eluting with methanol:DCM (0-10%) to give 612 mg (56%) of (3S,4S)-3-[1-isopropyl-3-methyl-bicyclo[3.2.1]-2-oxo-1β,3,8-triaza-spiro[4.5]dodec-8-ylmethyl]-4-phenyl-pyrrolidine-1-carboxylic acid tert-butyl ester as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076349B2
Source datasetuspto-grants-2011_12
ORD IDord-bc7132f6b17c4d51a4e4d70f91e5d231
Source noteuspto-grants-2011_12