HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Pentyn-1-ol → Tert-butyl 3-(3-(5-hydroxypent-1-ynyl)phenyl)propylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Pentyn-1-ol | HCID 79346 | — |
| Reactant | Tert-butyl 3-(3-bromophenyl)propylcarbamate | HCID 57219374 | — |
| Product | Tert-butyl 3-(3-(5-hydroxypent-1-ynyl)phenyl)propylcarbamate | HCID 66742928 | — |
Reaction Steps
Sonogashira reaction of bromide 57 with 4-pentyn-1-ol gave tert-butyl 3-(3-(5-hydroxypent-1-ynyl)phenyl)propylcarbamate as yellow oil. Yield (0.653 g, 59%): 1H NMR (400 MHz, CDCl3) δ 7.17-7.23 (m, 3H), 7.08 (d, J=7.2 Hz, 1H), 4.53 (bs, 1H), 3.83 (t J=6.0 Hz, 2H), 3.10-3.18 (m, 2H), 2.60 (t, J=7.8 Hz, 2H), 2.54 (t, J=7.0 Hz, 2H), 1.83-1.90 (m, 2H), 1.74-1.82 (m, 2H), 1.44 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076516B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-a9b7640f6a10427a9fb1cb57c8faa891 |
| Source note | uspto-grants-2011_12 |