HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isophorone → HCID 131720240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isophorone | HCID 6544 | — |
| Reactant | HCID 178488804 | HCID 178488804 | — |
| Product | HCID 131720240 | HCID 131720240 | 60% |
Reaction Steps
This compound was prepared from isophorone (0.168 g, 1.22 mmol) in the manner previously described for enone 13, affording 0.342 g (60%) of the alkylation product (Rf 0.40, 2:1 hexanes/ethyl acetate) as a colorless, oily solid. 1H NMR (400 MHz, CDCl3) δ0.20 and 0.22 [2s, 2×3H, Si(CH3)2 ], 0.99 [s, 9H, SiC(CH3)3 ], 1.00 and 1.02 (2s, 2×3H, geminal-CH3 's),b 1.91 (s, 3H, 3-CH3), 2.18 and 2.28 (ABq, 2H), 2.42 (dd, 1H), 2.82 (dd, 2H), 3.70 (s, 3H, OCH3), 5.82 (sl d, 1H, 2-H), 6.71 (s, 1H, 6'-H), 6.92 ppm (s, 1H, 3'-H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05677336 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-862c1340c5344140902b193d959d30cb |
| Source note | uspto-grants-1997_10 |