HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 67296450, compound → HCID 67313802, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 67296450 | HCID 67296450 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Product | HCID 67313802 | HCID 67313802 | — |
Reaction Steps
Oxidation of tert-butyl 3-(3-(cyclohexanecarboxamido)phenyl)-3-hydroxypropylcarbamate (37) following the method used in Example 12 except PCC was used in lieu of MnO2 gave tert-butyl 3-(3-(cyclohexanecarboxamido)phenyl)-3-oxopropylcarbamate as a white solid. Yield (0.36 g, 91%); 1H NMR (400 MHz, DMSO-d6) δ 9.97 (s, 1H), 8.15-8.18 (m, 1H), 7.82 (dd, J=1.2, 8.0 Hz, 1H), 7.57 (d, J=8.0 Hz, 1H), 7.40 (t, J=8.0 Hz, 1H), 6.79 (br.t, 1H), 3.24 (q, J=6.0 Hz, 2H), 3.08 (t, J=6.4 Hz, 2H), 2.25-2.35 (m, 1H), 1.69-1.82 (m, 4H), 1.58-1.66 (m, 1H), 1.33 (s, 9H), 1.10-1.44 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193669B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-5a1055f5d393452dba0e0fd3048f1700 |
| Source note | uspto-grants-2015_11 |