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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885497Generated: October 31, 2026

Benzoyl chloride → 2-(N-benzyloxycarbonylamino)-5-(N-benzylcarbonylamino)phenol

https://huagongshe.com/reaction/1885497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCalcium CarbonateHCID 10112—
Reactant5-Amino-2-(benzyloxycarbonylamino)phenolHCID 14745733—
Solvent1,4-DioxaneHCID 31275—
Product2-(N-benzyloxycarbonylamino)-5-(N-benzylcarbonylamino)phenolHCID 14745740—

Reaction Steps

12 g of benzoyl chloride are slowly added dropwise to 0.77 mole (20 g) of 5-amino-2-(benzyloxycarbonylamino)phenol (prepared in the 2nd stage of Example 1) and 12 g of calcium carbonate in 120 ml of dioxane brought to 80° C. The mixture is heated for a further 20 minutes after the addition is complete. The mixture is filtered while hot in order to remove the inorganic salts. The expected product is precipitated by diluting the filtrate with ice-cold water. When recrystallized from methoxyethanol, it melts at 252° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145483
Source datasetuspto-grants-1992_09
ORD IDord-b37f28bf79554056bc20012edc1a7fa2
Source noteuspto-grants-1992_09