HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889454Generated: October 30, 2026
Sodium Sulfate → N-[(4-methoxyphenyl)methyl]cyclobutanamine
https://huagongshe.com/reaction/889454
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Cyclobutylamine | HCID 75645 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Magnesium perchlorate | HCID 24840 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-[(4-methoxyphenyl)methyl]cyclobutanamine | HCID 59313984 | 95.8% |
Reaction Steps
4-Methoxybenzaldehyde (5.63 mL, 46.4 mmol) and cyclobutanamine (3.3 g, 46.4 mmol) in dichloromethane (40 mL) were stirred at room temperature. After 45 min., magnesium perchlorate (0.231 g, 2.320 mmol) was added, and the reaction mixture was stirred at room temperature. After 16 hours, the reaction mixture was treated with Na2SO4 (2 g) and stirred at room temperature for 2 hours, filtered and concentrated to dryness. The reaction mixture was dissolved in methanol (40 mL), cooled to 0° C., and NaBH4 (1.6 g, 69.6 mmol) was added. After 15 min., the reaction mixture was warmed to room temperature. After 2 hours, the reaction mixture was diluted with 1N NaOH (100 mL) and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over Na2SO4, filtered and concentrated to isolate 4A (8.5 g, 82% yield) as a clear oil. HPLC: Rt=0.82 min (PHENOMENEX® Luna 5 micron C18 4.6×30 mm, 10-90% aqueous methanol containing 0.1% TFA, 2 min gradient, flow rate=5 mL/min, detection at 254 nm). MS (ES): m/z=192.6 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252795B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-2f8ba0499ddc47018ec8122fd7fc370c |
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| Source note | uspto-grants-2012_08 |
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