HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47720Generated: October 30, 2026
Ethanol → Glycine, N-(m-nitrophenyl)-, ethyl ester
https://huagongshe.com/reaction/47720
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Glycine, N-(m-nitrophenyl)- | HCID 25089 | — |
| Solvent | Water | HCID 962 | — |
| Product | Glycine, N-(m-nitrophenyl)-, ethyl ester | HCID 19172 | — |
Reaction Steps
2 g of 3-nitrophenylglycine are heated for 20 hours with stirring at a temperature in the region of 100° C. in 100 cm3 of absolute ethanol containing 20 cm3 of 6.5N hydrochloric ethanol. The suspension is filtered at a temperature in the region of 50° C.; the filtrate is concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The residue obtained is taken up in water and then extracted with about 100 cm3 of ethyl acetate. The aqueous phase is made alkaline by addition of sodium carbonate until a pH in the region of 10 is obtained. The medium is extracted with ethyl acetate; the combined extracts are washed with aqueous sodium chloride solution, dried over magnesium sulfate and then concentrated under reduced pressure (5 kPa) at 40° C. 1 g of ethyl 3-nitrophenylglycinate is obtained in the form of a yellow oil. (Rf=0.38 in a 95/5 by volume mixture of dichloromethane/methanol, on a Merck 60F254R silica plate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06699895B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-bd901037b2d24274865054226e84c567 |
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| Source note | uspto-grants-2004_03 |
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