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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892934Generated: October 27, 2026

Potassium Acetate → ethyl N-[[5-(3-bromobenzoyl)-2-nitrophenyl]methyl]glycine

https://huagongshe.com/reaction/892934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant5-(3-Bromobenzoyl)-2-nitrobenzaldehydeHCID 15177127—
Reactant2-(Ethylamino)acetic acid hydrochlorideHCID 19011402—
ReactantSodium cyanoborohydride [MI]HCID 20587905—
SolventEthanolHCID 702—
Productethyl N-[[5-(3-bromobenzoyl)-2-nitrophenyl]methyl]glycineHCID 6788384756.2%

Reaction Steps

To a stirred mixture of 58.9 parts of potassium acetate, 100.5 parts of ethyl glycine monohydrochloride and 790 parts of ethanol, there were added 100 parts of 5-(3-bromobenzoyl)-2-nitrobenzaldehyde (prepared following the procedure described in Example 9 or Example 14. After stirring for 1/2 hour, there were added portionwise 9.4 parts of sodium cyanotrihydroborate. Stirring was continued for 1/2 hour at room temperature. The reaction mixture was evaporated and the residue was partitioned between water and dichloromethane. The organic layer was separated, washed with water, dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /C2H5OH 99:1). The eluent of the desired fraction was evaporated, yielding 71 parts (56.2%) of ethyl N-[[5-(3-bromobenzoyl)-2-nitrophenyl]methyl]glycine (interm. 66).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120845
Source datasetuspto-grants-1992_06
ORD IDord-07c20d547ff945f4bd910020b7d12891
Source noteuspto-grants-1992_06