HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445956Generated: October 25, 2026
Benzaldehyde → Ethyl 2-(benzylideneamino)acetate
https://huagongshe.com/reaction/1445956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | Ethyl N-phenylglycinate hydrochloride | HCID 12241367 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(benzylideneamino)acetate | HCID 357745 | 131.8% |
Reaction Steps
To a mixture of 10.6 g of ethyl phenylglycinate hydrochloride 2 (49.3 mmol), 100 mL of dichloromethane, 5 ml of benzaldehyde (49.2 mmol) and 30 g of magnesium sulfate (249.2 mmol) were added at room temperature, under a nitrogen atmosphere, 21.25 mL of triethylamine (152.46 mmol). After stirring for 17 h the heterogeneous reaction mixture was filtered through celite and the solid was washed with 100 mL of dichloromethane. The solvents were evaporated under reduced pressure and the viscous oil thus obtained was stirred with 80 mL of diethyl ether and 80 mL of water until dissolution. After decantation, the organic layer was dried over sodium sulphate and the solvent was evaporated under vacuum. The immine ester 3 (12.4 g, 94% yield) was obtained as a yellow pale oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666907B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-f913aea34d7d47dca9e591881e907db7 |
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| Source note | uspto-grants-2010_02 |
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