HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21266598, compound → HCID 21266606, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21266598 | HCID 21266598 | — |
| Reactant | HCID 21266613 | HCID 21266613 | — |
| Product | HCID 21266606 | HCID 21266606 | — |
Reaction Steps
Prepared via the 4,4-di-(2-tolyl)-1-butyliodide, 33a and isolated as an oil. 1H NMR (CDCl3) δ1.20 (s broad, 2H), 1.42-1.58 (m,2H), 1.87-2.03 (m,2H), 2.27 (s,6H), 2.70 (t,2H), 4.23 (t,1H), 7.05-7.16 (m,8H) 4,4-Di-(2-tolyl)-3-butenylamine, 30c. Prepared via the 4,4-di-(2-tolyl)-3-butenylodide 36a and isolated as an oil. 1H NMR (CDCl3) δ1.20 (s broad, 2H), 2.11 (s,3H), 2.18 (q,2H), 2.26 (s,3H), 2.77 (t,2H), 5.75 (t,1H), 7.02-7.18 (m,8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998613 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-7c9189450a35483e91ee7c31a66b13bf |
| Source note | uspto-grants-1999_12 |