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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119261Generated: October 30, 2026

Diethyl Ether → Di-tert-butyl (2-formyl-1,4-phenylene)dicarbamate

https://huagongshe.com/reaction/2119261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDimethylformamideHCID 6228—
Reactant2,5-Bis-tert.-butyloxycarbonylaminobromobenzeneHCID 15428967—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
ProductDi-tert-butyl (2-formyl-1,4-phenylene)dicarbamateHCID 15539052—

Reaction Conditions

Temperature-20 °C

Reaction Steps

3.3 g (0.01 mol) 2,5-bis-tert.-butyloxycarbonylamino-bromobenzene from step A are dissolved in 100 ml of water-free tetrahydrofuran under argon. Gradually 17 ml of a 1.6 molar methyl lithium ether solution (0.03 mol) are added. The reaction mixture is cooled to −20° C. Subsequently 7 ml of 1.5 molar t-butyl lithium solution (0.01 mol) are added gradually. After ending the addition the solution is stirred for 30 minutes at −20° C. Subsequently 1.2 g of dimethylformamide (0.02 mol) are added and the reaction mixture is stirred for an hour at −20° C. After slow heating to room temperature the reaction mixture is hydrolyzed with water and then poured into ether, the aqueous phase is extracted with ether and then the organic phase is dried with magnesium sulfate. The solvent is distilled off in a rotary evaporator and the residue is purified on silica gel with petroleum ether/ethyl acetate (9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06685751B2
Source datasetuspto-grants-2004_02
ORD IDord-7e197858ed614db0ac99b9ca2ecf2310
Source noteuspto-grants-2004_02