HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099700Generated: October 31, 2026
Hydrochloric Acid → Benzeneethanamine, 3,4-dimethoxy-N,alpha-dimethyl-
https://huagongshe.com/reaction/2099700
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-Propanone, 1-(3,4-dimethoxyphenyl)- | HCID 69896 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzeneethanamine, 3,4-dimethoxy-N,alpha-dimethyl- | HCID 12235308 | 92% |
Reaction Steps
A solution of 15.1 g (78 mmol) of (3,4-dimethoxyphenyl)acetone (1) in 102 mL of methanol was cooled to 4° C. and was treated with 35 mL of 40% aqueous methylamine. To the reaction mixture, 3.5 g (92.5 mmol) of sodium borohydride was then added, and the temperature of the reaction was maintained at 4° C. The reaction mixture was allowed to stir for an additional 30 minutes, then concentrated under reduced pressure. To the residue, 60 mL of water was added, and the resulting reaction mixture was acidified to pH 1 using 6N HCl. The aqueous layer was extracted with 5×50 mL of dichloromethane, and the pH was adjusted to pH 13 using 6N NaOH. The aqueous layer was extracted with 4×75 mL of dichloromethane. The organic layers were combined, dried and concentrated to give 15 g (72 mmol, 92%) of 1A as a colorless oil (M+H, 210).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569676B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-26b63cefb36f4547a85b06b7b0e4a423 |
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| Source note | uspto-grants-2009_08 |
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