Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | 1,12-Dibromododecane | HCID 18766 | — |
| Product | HCID 11786613 | HCID 11786613 | — |
Reaction Steps
1,12-Dibromododecane (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 off-white solid was isolated. 1H NMR (300 MHz, DMSO-D6) δ 10.06 (1H, d, C1-H), 8.78 (1H, d, C3-H), 8.58 (1H, d, C8-H), 8.48 (1H, d, C4-H), 8.35 (1H, d, C7-H), 8.25 (1H, t, C5-H), 8.07 (1H, t, C6-H), 4.70 (2H, t, C′1-CH2), 2.0 (2H, m, C′2-CH2), 1.75 (1H, m, C′3-CH2), 1.15-1.40 (7H, m, C′3-6-CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546415B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-66820bf80d4e4370b75982c01524f75b |
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| Source note | uspto-grants-2013_10 |
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