HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1989813Generated: October 29, 2026
Hydrochloric Acid → 5-Dibutylamino-2-methoxy-benzaldehyde
https://huagongshe.com/reaction/1989813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 2-(5-Bromo-2-methoxyphenyl)-1,3-dioxane | HCID 14378759 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Dibutylamino-2-methoxy-benzaldehyde | HCID 85888906 | 46% |
Reaction Steps
2-(5-Bromo-2-methoxy-phenyl)-[1,3]dioxane (40 mmol), di-n-butylamine (48 mmol), Pd2(dba)3 (0.2 mmol, 1 mol % Pd), P(o-tol)3 (0.6 mmol) and Na-t-OBu (68 mmol) was stirred in degassed toluene (60 mL) at 80° C. for 18 h. The darkbrown mixture was poured into icecold hydrochloric acid (1 M, 200 mL) and stirred vigorously for 2 hours at 25° C. The solution was cooled to 0° C. and pH was adjusted to 9 using 6M NaOH(aq) and extracted with Et2O (4×100 mL). The organic phase was dried (Na2SO4) and the solvent was removed under reduced pressure. The resulting crude oil purified by flash chromatography using EtOAc/n-heptane (1:4, v/v) as eluent. The product was isolated as yellow oil in 46% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07642367B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-8261bab93a224a1980c3988478e40b97 |
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| Source note | uspto-grants-2010_01 |
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