HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836462Generated: October 27, 2026
Sodium cyanoborohydride → Benzenemethanamine, 4-fluoro-N-methoxy-
https://huagongshe.com/reaction/1836462
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-Fluoro-benzaldehyde O-methyl-oxime | HCID 53963238 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Benzenemethanamine, 4-fluoro-N-methoxy- | HCID 12147060 | 75% |
Reaction Steps
In an alternative procedure a solution of 4-fluorobenzaldehyde O-methyloxime (0.82 g, 5.35 mmol) in acetic acid ( 8 ml ) was treated at 10° C. with sodium cyanoborohydride (0.67 g, 10.7 mmol) added in small portions over 10 min and the resulting solution was stirred at 25° C. for 18 h. The solvent was evaporated under reduced pressure (co-evaporation with toluene twice) and the residue was slurried with water and the pH was adjusted to 9 with 2 N aqueous sodium hydroxide. The aqueous phase was extracted twice with ether and the combined organic extracts were washed with brine, dried (magnesium sulfate) and concentrated under reduced pressure. The residual oil was chromatographed on silica gel (elution hexane-ethyl acetate, 8:2) and distilled in vacuo to give 0.62 g (75% yield) of the title amine as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06777440B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-9566c8a0c167463ea3cc97075fef2179 |
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| Source note | uspto-grants-2004_08 |
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