HuagongsheHuagongshe Chemistry Print Report · For research reference only
Decanal → HCID 14403850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Decanal | HCID 8175 | — |
| Reactant | HCID 14403835 | HCID 14403835 | — |
| Product | HCID 14403850 | HCID 14403850 | 38% |
Reaction Steps
In the manner described in Example 1, (E)-2-[2-(2-bromo-4,6-dimethylphenyl)ethenyl]-5,5-dimethyl-1,3-dioxane was reacted with n-decanal to obtain (E)-2-[2-(5,5-dimethyl-1,3-dioxan-2-yl)ethenyl]3,5-dimethyl-α-nonylbenzenemethanol as a white solid (955.4 mg, 38%): 59°-61° C.; IR (KBr) 3320, 2900, 2820, 1460 and 1375 cm-1 ; NMR (DMSO-d6) δ 0.72 (3H, s), 0.86 (3H, t, J=8 Hz), 1.14 (3H, s), 1.22 (14H, broad singlet), 1.40-1.56 (2H, m), 2.18 (3H, s), 2.26 (3H, s), 3.54 (2H, d, J=12 Hz), 3.64 (2H, d, J=12 Hz), 4.66-4.76 (1H, m), 4.90 (1H, d, J=5 Hz, exchangeable), 5.06 (1H, d, J=6 Hz), 5.58 (1H, dd, J=5, 15 Hz), 6.72 (1H, d, J=15 Hz), 6.92 (1H, s), 7.18 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04812583 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-74ae7508e32a4d57a2009a3b8cb5f58f |
| Source note | uspto-grants-1989_03 |