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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925274Generated: October 28, 2026

Chloride → N-(6-Hydroxy-naphthalen-1-yl)-benzamide

https://huagongshe.com/reaction/1925274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantWaterHCID 962—
Reactant5-Amino-2-naphtholHCID 6865—
ReactantPotassium CarbonateHCID 11430—
SolventDichloromethaneHCID 6344—
ProductN-(6-Hydroxy-naphthalen-1-yl)-benzamideHCID 67520279—

Reaction Steps

To a round bottom flask containing 1.00 g (6.3 mmol) 5-amino-naphthalene-2-ol in 10 mL CH2Cl2, was added 2.61 g (0.0189 mmol) K2CO3, followed by 1.46 mL (0.0126 mmol) benzolyl chloride. The solution mixture was stirred under inert atmosphere until completion. After stirring for 18 h, water was added into the mixture and diluted with CH2Cl2. The organics were separated by sep. funnel, while extracting the organics 3× with CH2Cl2. The organic layers were combined, dried over Na2SO4, filtered and concentrated in-vacuo. The crude was purified by crystallization in CH2Cl2/Hexanes. A gray colored powder was collected, which was titled compound. MS (ESI pos. ion) m/z: 264 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178557B2
Source datasetuspto-grants-2012_05
ORD IDord-8ff2bdf2772242e1b5a5d789e259eb82
Source noteuspto-grants-2012_05