HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromo-1-heptene → n-Methylhept-5-en-1-amine tosylate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromo-1-heptene | HCID 524450 | — |
| Reactant | N-methylhex-5-en-1-amine 4-methylbenzenesulfonate | HCID 46737741 | — |
| Product | n-Methylhept-5-en-1-amine tosylate salt | HCID 131729112 | — |
Reaction Steps
N-Methylhept-5-en-1-amine tosylate salt 31b was synthesized from 7-bromo-heptene, according to the procedure as described for compound 31a, as a white solid in quantitative yield. 1H NMR (CDCl3, 400 MHz) δ 1.38 (q, J=7.76 Hz, 2H), 1.71 (q, J=7.76 Hz, 2H), 1.80 (q, J=6.98 Hz, 2H), 1.99 (q, J=6.98 Hz, 2H), 2.38 (s, 3H), 2.70 (t, J=5.17 Hz, 3H), 2.87-2.93 (m, 2H), 4.92-4.99 (m, 2H), 5.67-5.73 (m, 1H), 7.20 (d, J=7.76 Hz, 2H), 7.75 (d, J=7.76 Hz, 2H), 8.62 (br s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284307B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-22256e22d95a436c90ab78d2893a3ae0 |
| Source note | uspto-grants-2016_03 |