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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49979Generated: October 27, 2026

Sodium hydride → (2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-proline

https://huagongshe.com/reaction/49979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant1-(tert-Butyl) 2-methyl (2S,4R)-4-hydroxy-2-methylpyrrolidine-1,2-dicarboxylateHCID 10635010—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-N-Boc-4-(4-Bromobenzyloxy)-2-methyl-prolineHCID 2130100528.4%

Reaction Steps

To a suspension of sodium hydride (60% in oil) (0.12 g) (1.5 eq.) in 5 mL of dry THF was added (2S,4R)-N-Boc-4-hydroxy-2-methyl-proline methyl ester (0.55 g) in 5 mL of dry THF. The reaction mixture was stirred for 45 min., and a solution of 4-bromobenzyl bromide (0.75 g) (1.5 eq.) in 5 mL of dry THF was added. The reaction mixture was refluxed for 3 h. After cooling to RT, the reaction mixture was diluted with water and extracted with EtOAc. The aqueous layer was acidified and extracted with DCM. The combined organic extracts were washed with water, dried over MgSO4 and evaporated under reduced pressure to afford (2S,4R)-N-Boc-4-(4-bromo-benzyloxy)-2-methyl-proline (0.25 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710064B2
Source datasetuspto-grants-2004_03
ORD IDord-2d29d28f58b24fcfa52d6529402a7cce
Source noteuspto-grants-2004_03