HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598475Generated: November 3, 2026
Benzaldehyde → (Benzylamino)acetaldehyde diethyl acetal
https://huagongshe.com/reaction/1598475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (Benzylamino)acetaldehyde diethyl acetal | HCID 521961 | — |
Reaction Steps
A solution of benzaldehyde (3.0 mL, 0.0295 mol) and 2-aminoacetaldehyde diethyl acetal (4.3 mL, 0.0295 mol) in dichloroethane (60 mL) was brought to pH 7 by the addition of acetic acid. Sodium triacetoxyborohydride (8.1 g, 0.038 mol) was added and the reaction stirred until complete. Saturated sodium bicarbonate was added and the reaction stirred for 30 min. Ethyl acetate was added and the organic phase washed with saturated sodium chloride, then dried over magnesium sulfate. The crude product was chromatographed on silica gel with 30% ethyl acetate in hexane. The title compound was obtained as a pale yellow oil (2.93 g). NMR (CDCl3, 300 MHz) δ 7.31 (5H, m), 4.62 (1H, t, J=5 Hz), 3.81 (2H, s), 3.68 (2H, m), 3.54 (2H, m), 2.75 (2H d, J=5 Hz), 1.20 (6H, t, J=7 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05736539 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-868e549ba226461c86cd20a9543d96fb |
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| Source note | uspto-grants-1998_04 |
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