Phthalic Anhydride → 2-[4-(4-Hydroxyphenyl)butyl]-1H-isoindole-1,3(2H)-dione

HRID 2220963Notes

Reaction equation

HRID 2220963 reaction equation
Br.[NH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1.[C:14]1(=O)[O:19][C:17](=[O:18])[C:16]2=[CH:20][CH:21]=[CH:22][CH:23]=[C:15]12.C(N(CC)CC)C>C(Cl)(Cl)Cl>[OH:13][C:10]1[CH:9]=[CH:8][C:7]([CH2:6][CH2:5][CH2:4][CH2:3][N:2]2[C:17](=[O:18])[C:16]3[C:15](=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:14]2=[O:19])=[CH:12][CH:11]=1

Participants

5

Procedure

A mixture of 4-(4-aminobutyl)phenol hydrobromide 6 (8.2 g, 33.5 mmol), phthalic anhydride 7 (5.0 g, 33.8 mmol), and triethylamine (4.6 mL, 33.5 mmol) in chloroform (50 mL) was stirred at reflux for 18 h, cooled to room temperature and concentrated by rotary evaporation. The residue was dissolved in. acetic acid (50 mL) and stirred at 100° C. for 3 h. Solvent was evaporated and the resulting residue was purified by flash silica gel column chromatography eluting with CH2Cl2/EtOAc/hexanes (8:1:1, v/v) to give the desired product 8 as a white powder (4.1 g, 41% yield). 1H NMR (300 MHz, DMSO-d6) δ 1.57 (m, 4H), 2.46 (m, 2H), 3.58 (m, 2H), 6.64 (d, 2H), 6.95 (d, 2H), 7.82 (m, 4H), 9.12 (s, 1H). m/z (ESI): 296 [C18H17NO3+H]+.

Workup

  1. temperatureat reflux for 18 h
  2. concentrationconcentrated by rotary evaporation
  3. dissolutionThe residue was dissolved in
  4. stirringacetic acid (50 mL) and stirred at 100° C. for 3 h
  5. customSolvent was evaporated
  6. customthe resulting residue was purified by flash silica gel column chromatography
  7. washeluting with CH2Cl2/EtOAc/hexanes (8:1:1

Sources & evidence

ORD record
ord-ff617a126c404199bd0ece2391f4ce52
Source dataset
uspto-grants-2008_05
Patent number
US07368451B2

Reaction notes

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