HCID 66577527, compound → 3,4,4a,5,6,7-hexahydro-1H-isochromene
Reaction equation
C=[C:2]1[CH:7]([CH2:8][CH2:9][CH2:10][CH:11]=C)[CH2:6][CH2:5][O:4][CH2:3]1>C(Cl)Cl>[CH2:3]1[C:2]2[CH:7]([CH2:8][CH2:9][CH2:10][CH:11]=2)[CH2:6][CH2:5][O:4]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
3-methylidene-4-(pent-4-en-1-yl)tetrahydro-2H-pyran (1320 mg, 7.94 mmol) was added to CH2Cl2 (159.00 ml) at RT. The reaction was degassed three times. Zhan-1b (58.3 mg, 0.079 mmol) was added at 0° C. The reaction mixture was degassed again and then stirred at room temperature for 1 h. The mixture was concentrated under reduced pressure (280 mmhg). The residue was purified by column chromatography on silica gel to provide the title compound. 1H NMR (500 MHz, CDCl3) δ 5.54 (d, 1H, J=2.2 Hz), 4.06 (d, 1H, J=122 Hz), 3.97 (dd, 1H, J=4.4 Hz, 11.2 Hz), 3.84-3.91 (m, 1H), 3.46-3.53 (m, 1H), 2.21 (bs, 1H), 1.92-2.19 (m, 2H), 1.80-1.89 (m, 1H), 1.68-1.86 (m, 2H), 1.36-1.48 (m, 2H), 1.16-1.26 (m, 1H).
Workup
- customThe reaction was degassed three times
- additionZhan-1b (58.3 mg, 0.079 mmol) was added at 0° C
- customThe reaction mixture was degassed again
- concentrationThe mixture was concentrated under reduced pressure (280 mmhg)
- customThe residue was purified by column chromatography on silica gel
Sources & evidence
- ORD record
- ord-54684b908c674e9192b7872bf42c6832
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08829196B2
Reaction notes
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