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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036740Generated: October 29, 2026

Sodium hydride → HCID 59976013, compound

https://huagongshe.com/reaction/1036740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzyl bromideHCID 68021—
Reactant(R)-2-tert-butoxycarbonylamino-3-hydroxy propionic acidHCID 637603—
SolventDimethylformamideHCID 6228—
ProductHCID 59976013HCID 59976013—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N—BOC-D-serine (2.00 g, 9.75 mmol) in DMF (25 ml) was cooled to 0° C. under nitrogen atmosphere and sodium hydride (60% in mineral oil) (0.82 g, 20.47 mmol) was added portionwise over 15 minutes. After stirring at 0° C. for 30 minutes, 4-fluorobenzyl bromide (1.82 g, 9.75 mmol) in DMF (5 ml) was added. The ice bath was removed and the reaction mixture was stirred at room temperature overnight. The reaction mixture was partitioned between EtOAc (100 ml) and water (50 ml). The aqueous phase was separated and washed with DCM (2×50 ml). The organic washings were discarded. The aqueous layer was acidified with 5% citric acid aqueous solution and back-extracted with DCM (2×100 ml). The combined organic portions were washed with brine (50 ml), dried (MgSO4) and concentrated in vacuo to yield the title compound as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546416B2
Source datasetuspto-grants-2013_10
ORD IDord-969bcfdd359a4d338a21cb58333f7126
Source noteuspto-grants-2013_10