Tributylstannane → HCID 69110671, compound

HRID 2427764Notes

Reaction equation

HRID 2427764 reaction equation
Br[C:2]1[C:10]([O:11][CH3:12])=[CH:9][C:8]([O:13][CH3:14])=[C:7]2[C:3]=1[CH2:4][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=1)[C:6]2=O.C([SnH](CCCC)CCCC)CCC.[F-].[K+]>C1C=CC=CC=1>[CH3:12][O:11][C:10]1[CH:2]=[C:3]2[C:7](=[C:8]([O:13][CH3:14])[CH:9]=1)[CH2:6][N:5]([CH2:16][C:17]1[CH:22]=[CH:21][C:20]([Cl:23])=[CH:19][CH:18]=1)[CH2:4]2

Participants

5

Reactant 3

HCID 5948TributylstannaneHCID 522689Potassium FluorideHCID 66890021HCID 66890021, compound

Product 1

HCID 69110671HCID 69110671, compoundYield 46.1%

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

To a solution of 4-bromo-5,7-Dimethoxy-2-(4-chloro-benzyl)-2,3-dihydro-isoindol-1-one (0.100 g, 0.25 mmol) in benzene under N2 atmosphere was added 2,2′-azobis(2-methyl propionitrile) AIBN (5.0 mg), followed by tributyl tin hydride (0.132 mL, 0.5 mmol). The resulting mixture was refluxed in an oil bath for 2 h. The reaction was monitored by GC-MS for the disappearance of starting material. The reaction mixture was cooled to room temperature and stirred with potassium fluoride (200 mg) for 45 min. The solids were filtered and the filtrate was concentrated. The resulting material was purified using column chromatography (typically 40% ethyl acetate in hexanes) to give 5,7-Dimethoxy-2-(4-chloro-benzyl)-2,3-dihydro-isoindol-lone (0.035 g, 44%). 1H NMR (300 MHz, CDCl3): δ (ppm) 3.82 (s, 3H), 3.95 (s, 3H), 4.15 (s, 2H), 4.69 (s, 2H), 6.43 (d, 2H), 7.25 (m, 4H). GC-MS: m/z 317 (M)+, 299 (M−18)+.

Workup

  1. temperatureThe resulting mixture was refluxed in an oil bath for 2 h
  2. filtrationThe solids were filtered
  3. concentrationthe filtrate was concentrated
  4. customThe resulting material was purified

Sources & evidence

ORD record
ord-32384a99170646c794e3d4fd77f5a546
Source dataset
uspto-grants-2011_06
Patent number
US07968570B2

Reaction notes

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