HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86761366, compound → HCID 86761367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86761366 | HCID 86761366 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86761367 | HCID 86761367 | 95% |
Reaction Steps
To a stirred mixture of tert-butyl [1-(benzyloxymethyl)tricyclo[3.3.1.03,7]non-3-yl]carbamate (1.0 g, 2.8 mmol) obtained in step V in MeOH (11 mL), Pd/C (10%, 0.2 g) was added. The H2 pressure was then applied with the balloon for 2 h. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated under reduced pressure to obtain tert-butyl [1-(hydroxymethyl)tricyclo[3.3.1.03,7]non-3-yl]carbamate as a viscous liquid (0.7 g) in 95% yield. m/z (M+1) 268; 1H NMR (CDCl3) 300 MHz δ 4.74 (s (br), 1H), 3.45 (s, 2H), 2.50-2.40 (m, 1H), 2.40-2.33 (m, 1H), 2.05-1.87 (m, 4H), 1.80 (dd, J=2.4, 10.3 Hz, 1H), 1.65 (dd, J=3.0, 10.0 Hz, 1H), 1.54-1.40 (m, 3H), 1.45 (s, 9H), 1.37 (dd, J=3.1, 10.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07985759B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-0ddc59525c284f80a492af9d29c30b63 |
| Source note | uspto-grants-2011_07 |