Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | HCID 22676876 | HCID 22676876 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22676882 | HCID 22676882 | 94% |
Reaction Steps
General procedure B using (S)-p-tol-BfNAP and 3-benzyloxybutyl-cyclopent-2-enone (0.146 g, 0.6 mmol) gave, after 30 h at 0° C. and flash chromatography (1:2 pentane:diethyl ether), the title compound as a clear oil (0.139 g, 94% yield). 1H NMR (300 MHz, CDCl3): δ7.37-7.23 (m, 5 H), 4.50 (s, 2 H), 3.47 (t, J=6.3 Hz, 2 H), 2.43-2.04 (m, 5 H), 1.78 (ddd, J=18.0, 9.6, 1.2 Hz, 1 H), 1.70-1.56 (m, 2 H), 1.56-1.34 (m, 5 H). 13C NMR (75 MHz, CDCl3): δ219.8, 138.6, 128.4, 127.7, 127.6, 73.1, 70.3, 45.4, 38.7, 37.4, 35.7, 30.0, 29.7, 24.8. IR (neat): 2934, 2860, 1741, 1455, 1405, 1363, 1158, 1100, 737, 699 cm−1. HRMS m/z calcd for C16H22O2 246.1620, obsd 246.1615. [α]D25° C.−89° (c 1.4, CHCl3). Chiral HPLC analysis (Chiracel OD column) indicated that the title compound was obtained in 94% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06465664B1 |
|---|
| Source dataset | uspto-grants-2002_10 |
|---|
| ORD ID | ord-082e2e706c23443aa7a54032770023a9 |
|---|
| Source note | uspto-grants-2002_10 |
|---|