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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846589Generated: October 31, 2026

Hydrogen Peroxide → trans-(7-Carbamoyl-1,1-diethyl-3-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1846589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 66673896HCID 66673896—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventIsopropyl AcetateHCID 7915—
SolventSodium PyrosulfiteHCID 656671—
Producttrans-(7-Carbamoyl-1,1-diethyl-3-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl)-carbamic acid tert-butyl esterHCID 66673985104%

Reaction Steps

To a solution of trans-(7-cyano-1,1-diethyl-3-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-carbamic acid tert-butyl ester (8.5 g, 24 mmol) in DMSO (105 mL) was added K2CO3 (4.98 g, 36 mmol), and the mixture was stirred until all solids were dissolved. To the solution was added 30% hydrogen peroxide (12.2 mL, 120 mmol) in 0.5 mL portions over 45 min at a rate to keep the temperature 30-35° C. The reaction mixture was diluted with water (200 mL) and isopropyl acetate (500 mL), and sodium metabisulfite was added (10 g) to reduce excess peroxides. Layers were separated and the aqueous layer was extracted with isopropyl acetate (3×150 mL) and 10% MeOH/isopropyl acetate (2×100 mL). The combined organic layers were washed with water (3×150 mL) and saturated NaCl (100 mL), dried with Na2SO4 and concentrated to give the title compound (9.4 g). (m/z): [M+H]+ calcd for C21H32N2O4 377.24; found 377.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952031B2
Source datasetuspto-grants-2015_02
ORD IDord-bd655931e84a4936869970cce97c9654
Source noteuspto-grants-2015_02