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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417373Generated: October 30, 2026

Ethyl bromoacetate → HCID 66625110, compound

https://huagongshe.com/reaction/417373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (4-aminophenyl)carbamateHCID 688611—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66625110HCID 6662511094%

Reaction Steps

Step A To a solution of N-Boc-1,4-phenylene diamine (Aldrich, 1.00 g, 4.82 mmol) in CH2Cl2 (12 ml) were added N,N-diisopropylethylamine (1.26 g, 9.76 mmol) and ethyl bromoacetate (Aldrich, 813 mg, 4.87 mmol). The mixture was allowed to stir at rt overnight and then taken up in EtOAc (300 ml) and washed with sat. aqueous Na2CO3, water and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give ethyl 2-(4-(tert-butoxycarbonylamino)phenylamino)acetate as a light brown oil (1.33 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088815B2
Source datasetuspto-grants-2012_01
ORD IDord-2bc3a7a169a64e9a85d92dcb2646ffeb
Source noteuspto-grants-2012_01