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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976494Generated: October 30, 2026

Benzyl chloroformate → HCID 21845734, compound

https://huagongshe.com/reaction/976494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant7-Aminonaphthalene-2-sulfonic acidHCID 68124—
ReactantSodiumHCID 5360545—
SolventWaterHCID 962—
ProductHCID 21845734HCID 21845734—

Reaction Steps

To a suspension of 7-aminonaphthalene-2-sulfonic acid, sodium salt (3.0 g, 12.2 mmol) in 70 mL of water is added solid NaOH (0.98 g, 24.0 mmol) at room temperature. The mixture is stirred for 30 minutes, and benzyl chloroformate (3.43 mL, 24.0 mmol) is then added. The resulting mixture is stirred over a period of 16 hours. The crude product is treated as in EXAMPLE 9, Part A, to give 4.18 g of crude N-CBz-7-aminonaphthalene-2-sulfonic acid, sodium salt. A mixture of the sulfonic acid, sodium salt (4.18 g, 11.0 mmol) in 12 mL of thionyl chloride is heated at 80° C. for 3 hours. The mixture is allowed to cool to room temperature and concentrated in vacuo. The residue is diluted with EtOAc and washed successively with water (2×), saturated NaHCO3 solution and saturated NaCl. The organic layer is dried over anhydrous MgSO4, filtered and concentrated to give a brown oil. The crude product is purified by column chromatography in a gradient of 10% EtOAc/hexanes to 30% EtOAc/hexanes to afford the title compound (1.76 g, 4.68. mmol) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612353
Source datasetuspto-grants-1997_03
ORD IDord-57f2a8edff2e4cf28b18bc80b09de558
Source noteuspto-grants-1997_03