HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686124Generated: November 1, 2026
Hydrochloric Acid → 2-Methoxy-4-methylbenzenemethanamine
https://huagongshe.com/reaction/1686124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 2-Methoxy-4-methylbenzamide | HCID 21947397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-4-methylbenzenemethanamine | HCID 58607466 | 64% |
Reaction Steps
To a solution of 2-methoxy-4-methylbenzamide (14.55 g, 88.08 mmol) in dry THF (50 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 220 mL, 2.5 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq. HCl (6 N, 37 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to give 8.5 g of (2-methoxy-4-methylphenyl)methanamine. (64% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148536B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-34eb81c691bd47b19c943fd3c8e8e348 |
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| Source note | uspto-grants-2012_04 |
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