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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400250Generated: November 3, 2026

Cesium carbonate → HCID 86709751, compound

https://huagongshe.com/reaction/1400250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-Chloro-2-naphtholHCID 12459—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantCarbamic acid, N-(2-bromo-1,1-dimethylethyl)-, 1,1-dimethylethyl esterHCID 74788455—
SolventAcetonitrileHCID 6342—
ProductHCID 86709751HCID 8670975151%

Reaction Steps

To a solution of 1-chloronaphthalen-2-ol (1.5 mmol) and Cs2CO3 (3 mmol) in acetonitrile was added tert-butyl (1-bromo-2-methylpropan-2-yl)carbamate (3 mmol). The resulting mixture was heated at reflux overnight. After TLC control (n-hexane/ethyl acetate 7:3) showed the disappearance of 1-chloronaphthalen-2-ol, solvent was evaporated in vacuo and the residue was dissolved in 15 mL of ethyl acetate and washed with water (3×5 mL), brine (10 mL) and dried over Na2SO4. The evaporation of solvent afforded tert-butyl {1-[(1-chloronaphthalen-2-yl)oxy]-2-methylpropan-2-yl}carbamate as a pale oil (51% yield) which was dissolved in 5 mL of 4 M HCl solution in dioxane. The resulting mixture was stirred at room temperature for 18 h. After HPLC-MS control, the solvent was distilled off and the residue was dissolved in dichloromethane and wash 2 times with NaOH 1N to afford 1-[(1-chloronaphthalen-2-yl)oxy]-2-methylpropan-2-amine as a pale oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906946B2
Source datasetuspto-grants-2014_12
ORD IDord-b1fcb02dc3a649d1907bfac3f2fd8edb
Source noteuspto-grants-2014_12