HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716792Generated: October 30, 2026
Benzaldehyde → 3-(3-(Benzylamino)phenyl)-3-hydroxypropanenitrile
https://huagongshe.com/reaction/716792
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-(3-Aminophenyl)-3-hydroxypropanenitrile | HCID 59316960 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(3-(Benzylamino)phenyl)-3-hydroxypropanenitrile | HCID 67296728 | — |
Reaction Steps
NaBH(OAc)3 (7.84 g, 36.99 mmol) was added to a solution of aniline 12 (2.0 g, 12.33 mmol) and benzaldehyde (1.3 g, 12.33 mmol) in DCM. The resulting mixture was stirred at RT for 5 h and quenched with saturated aqueous NaHCO3. Organic layer was washed with water followed by brine and dried over anhydrous Na2SO4. Organic layer was concentrated under reduced pressure. Purification by flash chromatography (40% to 50% EtOAc—hexanes gradient) gave 3-(3-(benzylamino)phenyl)-3-hydroxypropanenitrile as a pale yellow oil. Yield (2.61 g, 83%); 1H NMR (400 MHz, DMSO-d6) δ 7.36-7.29 (m, 4H), 7.23-7.19 (m, 1H), 6.99 (t, J=8.0 Hz, 1H), 6.68 (s, 1H), 6.54 (d, J=7.6 Hz, 1H), 6.44 (dd, J=1.6, 8.0 Hz, 1H), 6.27 (t, J=6.0 Hz, 1H), 5.79 (d, J=4.4 Hz, 1H), 4.72-4.68 (m, 1H), 4.25 (d, J=6.0 Hz, 2H), 2.82-2.67 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193669B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-06dbc9892d76453b8558a4eaaa315c1b |
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| Source note | uspto-grants-2015_11 |
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