Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | 1,10-Diiododecane | HCID 85378 | — |
| Product | HCID 11787103 | HCID 11787103 | 92% |
Reaction Steps
1,10-Diiododecane (mmol) was added to a solution (30 mL) of isoquinoline, and the solution heated for 24 hours at 65° C. The resulting precipitate was filtered, and the product washed five times with dry diethyl ether. The resulting yellow solid was isolated in a 92% yield. 1H NMR (300 MHz, DMSO-D6) δ 10.07 (1H, d, C1-H), 8.78 (1H, d, C3-H), 8.58 (1H, d, C8-H), 8.48 (1H, d, C4-H), 8.36 (1H, d, C7-H), 8.26 (1H, t, C5-H), 8.07 (1H, t, C6-H), 4.69 (2H, t, C′1-CH2), 2.0 (2H, m, C′2-CH2), 1.15-1.50 (6H, m, C′3-5-CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08546415B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-e731bab0088d48219dc5f08a065bd420 |
|---|
| Source note | uspto-grants-2013_10 |
|---|