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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898886Generated: October 31, 2026

Acetic Acid → HCID 68862803, compound

https://huagongshe.com/reaction/898886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthylamineHCID 6341—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant6-Methoxy-1,2,3,4-tetrahydronaphthalen-2-oneHCID 75582—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 68859918HCID 68859918—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 68862803HCID 6886280348%

Reaction Steps

To a mixture of 6-methoxy-2-tetralone (950 mg; 5.39 mmol), 2 M of ethylamine in THF (5.4 mL; 10.78 mmol) and acetic acid (648 mg; 10.78 mmol) in CH2Cl2 (5 mL) was added sodium triacetoxyborohydride (2.29 g; 10.78 mmol). The reaction mixture was stirred at RT for 3 h, then 1N solution of NaOH was added, and extracted with ether (3 times). The combined organic extracts were dried over Na2SO4, and the solvent was removed under reduced pressure to give a light-yellow oil. This oil was added to a solution of carbonic acid 1-chloro-ethyl ester 4-trifluoromethoxy-phenyl ester (1.23g; 4.31 mmol) in toluene(8 mL), and the reaction mixture was stirred for 1 h at RT followed by 1 h at 90° C. The reaction was allowed to cool to RT, diluted with Et2O and washed with 1 N of aqueous HCl and saturated NaHCO3. The organic extract was dried over Na2SO4, and the solvent was removed under reduced pressure. Flash chromatography of the residue with a gradient of hexane-CH2Cl2 gave 1.05 g (48%) of ethyl-(6-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-carbamic acid 4-trifluoromethoxy-phenyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351857B2
Source datasetuspto-grants-2008_04
ORD IDord-9e107006383043709bd6d9359606a419
Source noteuspto-grants-2008_04