HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021197Generated: November 4, 2026
2,5-Dimethoxy-3,4,6-trimethylbenzaldehyde → HCID 86653771, compound
https://huagongshe.com/reaction/1021197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dimethoxy-3,4,6-trimethylbenzaldehyde | HCID 2752605 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86653771 | HCID 86653771 | — |
Reaction Steps
A stirred solution of 2,5-dimethoxy-3,4,6-trimethylbenzaldehyde (6.34 g) in 125 mL THF was cooled to 0° C. and treated with 34 mL 1.0 M allyl magnesium bromide (1.0 M in THF, 1.1 equiv.) slowly over 0.25 h via dropping funnel. The solution was stirred for and additional 0.25 h and quenched by the addition of 40 mL 1.0 M aqueous citric acid and stirring until the layers clarified. The layers were separated and the aqueous layer extracted 3×50 mL EtOAc. The combined organics were washed 2×25 mL saturated aqueous NaCl, dried over Na2SO4 and concentrated to yield 9.8 g of 1-(2,5-dimethoxy-3,4,6-trimethylphenyl)but-3-en-1-ol as a brown oil. M+−H2O=233.4 m/z; 1H NMR (400 MHz, CDCl3) δ=5.90 (m, 1 H), 5.15 (m, 1 H), 5.10 (m, 1 H), 4.98 (m, 1 H), 3.78 (s, 3 H), 3.65 (s, 3 H), 2.66 (s, 1 H), 2.48 (s, 1 H), 2.25 (s, 3 H), 2.18 (s, 6H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08716527B2 |
|---|
| Source dataset | uspto-grants-2014_05 |
|---|
| ORD ID | ord-a34f093344424a789ebedc4e0f14b13a |
|---|
| Source note | uspto-grants-2014_05 |
|---|