HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722447Generated: October 30, 2026
N-(4-Methoxybenzylidene)glycine methyl ester → N-((4-Methoxyphenyl)methyl)glycine methyl ester
https://huagongshe.com/reaction/722447
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(4-Methoxybenzylidene)glycine methyl ester | HCID 4193973 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-((4-Methoxyphenyl)methyl)glycine methyl ester | HCID 10846084 | — |
Reaction Steps
To a solution of 91.3 g (0.441 mol) of [(4-methoxy-benzylidene)-amino]-acetic acid methyl ester in 500 ml of THF and 1000 ml of MeOH, 20 g (0.529 mol) of sodium borohydride is added portionwise at −10 to 0° C. The reaction mixture is stirred for 30 min. at −10 to 0° C. and quenched with sat. NH4Cl. After adding of ice-water, the mixture is concentrated to ¼ of whole volume and extracted with AcOEt. The combined extracts are washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure to give (4-methoxybenzylamino)-acetic acid methyl ester; NMR (CDCl3): 1.87 (br s, 1H), 3.41 (s, 2H), 3.73 (s, 3H), 3.74 (s, 2H), 3.8 (s, 3H), 6.86 (d, 2H, J=8.56 Hz), 7.24 (d, 2H, J=8.56 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07138432B1 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-a9b116057f5043d9acdbe7f7a69de1ee |
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| Source note | uspto-grants-2006_11 |
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