HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590790Generated: October 27, 2026
Acetic Acid → (S)-methyl 2-(bis(4-methoxybenzyl)amino)-2-phenylacetate
https://huagongshe.com/reaction/590790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (S)-methyl 2-((4-methoxybenzyl)amino)-2-phenylacetate | HCID 94161236 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | (S)-methyl 2-(bis(4-methoxybenzyl)amino)-2-phenylacetate | HCID 118272340 | 66% |
Reaction Steps
To a solution of (S)-methyl 2-((4-methoxybenzyl)amino)-2-phenylacetate (1.6 g, 5.61 mmol) in anhydrous dichloroethane (20 mL) was added 4-methoxy benzaldehyde (0.76 g, 5.61 mmol) and few drops of HOAc. After 30 min, the reaction mixture was cooled to 0° C., sodium triacetoxy borohydride (2.38 g, 11.22 mmol) was added and the contents were allowed to stir at ambient temperature. After 2 h, the reaction was quenched with ice cold H2O (10 mL), and the organic contents were extracted with CH2Cl2 (2×25 mL). The combined organic extracts were washed with brine (1×20 mL), dried over Na2SO4, concentrated and the residue thus obtained was purified by flash column chromatography to afford the title compoundas pale yellow liquid (1.5 g, 66%). MS ES+APCI calc'd. for C25H27NO4 [M+H]+ 406. Found 406.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09233979B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-8d14263a40c847cc86b8e4478216cb05 |
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| Source note | uspto-grants-2016_01 |
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