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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182615Generated: November 2, 2026

Methanol → Boc-(R)-alpha-(4-bromobenzyl)proline

https://huagongshe.com/reaction/2182615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantLithium HydroxideHCID 3939—
ReactantTetrahydrofuranHCID 8028—
ReactantN-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline ethyl esterHCID 69212228—
SolventWaterHCID 962—
ProductBoc-(R)-alpha-(4-bromobenzyl)prolineHCID 2761850108%

Reaction Steps

A mixture of N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline ethyl ester (3.00 g), LiOH (10 mmol), THF (25 mL), MeOH (10 mL) and H2O (5 mL) was stirred at room temperature overnight. The mixture was then heated at 74° C. overnight. The mixture was concentrated in vacuo, and water was added. The mixture was washed with Et2O and the aqueous layer was made acidic with the addition of 1N H2SO4. The aqueous layer was extracted with EtOAc. The EtOAc layer was washed with brine, dried over Na2SO4, and evaporated to give N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline (3.02 g). MS (m/z) 284 (MH+-t-Boc); mp: 143.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897225B1
Source datasetuspto-grants-2005_05
ORD IDord-76ba3c8e568549a2809cf05b71b54723
Source noteuspto-grants-2005_05