HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Benzyloxy-1-propanol → HCID 58880102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Benzyloxy-1-propanol | HCID 347971 | — |
| Reactant | HCID 58880184 | HCID 58880184 | — |
| Catalyst | HCID 178506449 | HCID 178506449 | — |
| Product | HCID 58880102 | HCID 58880102 | — |
Reaction Steps
The title compound was synthesized from Compound 247 and 3-(benzyloxy)propan-1-ol using an analogous procedure to that outlined in the preparation of Compound 210 followed by debenzylation using Pd/C—H2. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.16 (t, J=7.33 Hz, 3H) 1.99-2.06 (m, 2H) 2.25 (s, 3H) 3.41 (q, J=7.58 Hz, 2H) 3.71 (br. s., 2H) 4.26 (t, J=6.44 Hz, 2H) 4.81 (br. s., 1H) 7.23 (s, 1H) 7.46 (s, 1H) 7.87 (t, J=7.71 Hz, 1H) 8.03 (t, J=7.20 Hz, 2H) 8.11 (s, 1H) 8.31 (s, 1H) 12.27 (br. s., 1H); [M+H] calc'd for C23H24ClN2O4S, 459.1; found, 459.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318939B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-7edbc4f44c9c4f059018ad2c3c07f543 |
| Source note | uspto-grants-2012_11 |