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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264574Generated: October 31, 2026

Sodium hydride → HCID 86755435, compound

https://huagongshe.com/reaction/1264574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantalpha-Bromo-2-nitrotolueneHCID 77569—
Reactant3-Hydroxy-2-(4-methoxybenzenesulfonylamino)-propionic acid tert-butyl esterHCID 53978084—
SolventDimethylformamideHCID 6228—
ProductHCID 86755435HCID 86755435129.1%

Reaction Steps

To 6.16 g (18.6 mmol) of 3-hydroxy-2-(4-methoxybenzenesulfonylamino)-propionic acid tert-butyl ester in 50 ml of N,N-dimethylformamide, cooled in an ice bath, was added 0.781 g (19.5 mmol) of sodium hydride. After gas evolution ceased, a solution of 4.02 g (18.6 mmol) of 2-nitrobenzylbromide in 18 ml of N,N-dimethylformamide was added dropwise. The mixture was stirred under nitrogen at room temperature for 4 hours and 1.0 g of 2-nitrobenzyl bromide was added. The mixture was stirred at room temperature overnight and the solvent removed under vacuum. The residue was diluted with water and extracted with CH2Cl2. The organic extract was washed with H2O, brine and dried with Na2SO4. The solvent was removed to give 11.2 g of solid which was chromatographed on silica gel with hexane-ethyl acetate (1:1) as eluent followed by hexane-ethyl acetate (35:65) as eluent. The fractions containing product were combined and the solvent was then removed to gave 7.7 g (89%) of solid. A sample from a 3 mmol run gave a gum. Anal. for C21H26N2O8S: Calc'd: C, 54.1; H, 5.6; N, 6.0; Found: C, 54.0; H, 5.7; N, 6.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544984B1
Source datasetuspto-grants-2003_04
ORD IDord-40c75c21d8984df291d37751cf8ee7fc
Source noteuspto-grants-2003_04