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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 5-(3-Bromobenzoyl)-2-nitrobenzaldehyde | HCID 15177127 | — |
| Reactant | 2-(Ethylamino)acetic acid hydrochloride | HCID 19011402 | — |
| Reactant | Sodium cyanoborohydride [MI] | HCID 20587905 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl N-[[5-(3-bromobenzoyl)-2-nitrophenyl]methyl]glycine | HCID 67883847 | 56.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05120845 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-07c20d547ff945f4bd910020b7d12891 |
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| Source note | uspto-grants-1992_06 |
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