HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515487Generated: October 29, 2026
Hydrochloric Acid → 3-{[(4-Methoxyphenyl)methyl]amino}propan-1-ol
https://huagongshe.com/reaction/515487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-{[(4-Methoxyphenyl)methyl]amino}propan-1-ol | HCID 5100981 | 42% |
Reaction Steps
To a solution of 3-amino-propan-1-ol (15.0 g, 200 mmol) in methanol (300 ml) was added para-methoxybenzaldehyde (28.6 g, 210 mmol) and a few drops of acetic acid at room temperature. The mixture was stirred at room temperature for 2 hours and cooled to 0° C. After the addition of sodium borohydride (11.4 g, 300 mmol), the mixture was stirred at room temperature for another 2 hours and acidified with 3N hydrochloric acid. The biphasic mixture was stirred at room temperature for 10 minutes. The organic solvent was evaporated under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous phase was washed with ethyl acetate and basified with 6N sodium hydroxide. Extraction with chloroform was performed and the organic phase was dried over sodium sulfate followed by concentration in vacuo to afford 3-(4-methoxy-benzylamino)-propan-1-ol as pale yellow oil (16.4 g, 42%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108957B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-6a886eccc8d344bd925a7d6489568f0f |
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| Source note | uspto-grants-2015_08 |
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