Phthalimide → HCID 118931318, compound

A mixture of π-allylpalladium chloride dimer 0.4 mol % (20 mg, 53 μmol), 1.2 mol % (R,R)-DACH ligand (125 mg, 158 μmol, Na2CO3 (70 mg, 0.66 mmol) and phthalimide (1.94 g, 13.2 mmol) in 100 mL of dry CH2Cl2 was purged with nitrogen for 1 h. The resulting mixture was stirred for 10 min at room temperature to which butadiene monoepoxide (FIG. 2, No. 2) (920 mg, 13.2 mmol) was added. The resulting mixture was stirred at room temperature under nitrogen for 14 h, concentrated in vacuo and purified by silica gel column chromatography using ethyl acetate/hexane (3:7) as eluent furnished 2.8 g (98%) yield of (S)-2-(Isoindolin-2-yl) but-3-en-1-ol (FIG. 2, No. 3) as a crystalline white solid. [Rf=0.21, ethyl acetate/hexane (3:7)]; [α]D25 −72.2 (c 2.02, CH2Cl2) [Lit. −72.2 (c 2.02, CH2Cl2)]; IR (CH2Cl2) v: 3467, 1773, 1698, 1467, 1383 cm−1; 1H NMR (400 MHz, CDCl3) δ: 2.7 (bs, 1H), 3.9 (m, 1H), 4.1 (m, 1H), 4.9 (m, 1H), 5.2 (m, 2H), 6.1 (ddd, J=6.4 Hz, 1H), 7.7 (dd, J=3.2, 5.48 Hz, 2H), 7.8 (dd, J=2.76, 5.48 Hz, 2H); 13C NMR (100 MHz, CDCl3) δ: 55.9, 62.8, 118.8, 123.4, 131.7, 131.9, 134.2, 168.5. (Ref: Trost, B. M et al. J. Am. Chem. Soc. 2000, 122, 5968-597).

1. customwas purged with nitrogen for 1 h
2. addition2) (920 mg, 13.2 mmol) was added
3. stirringThe resulting mixture was stirred at room temperature under nitrogen for 14 h
4. concentrationconcentrated in vacuo
5. custompurified by silica gel column chromatography

ORD record

ord-4b1e6e038dc94930b5dcc38eb83e330d

Source dataset

uspto-grants-2016_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09284263B1