1,2-Dichloroethane → (2,4-Bis-benzyloxy-5-isopropenyl-phenyl)-(5-bromo-1,3-dihydro-isoindol-2-yl)-methanone

HRID 644653Notes

Reaction equation

HRID 644653 reaction equation
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([C:18]([CH3:20])=[CH2:19])=[CH:14][C:10]=1[C:11]([OH:13])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Br:21][C:22]1[CH:23]=[C:24]2[C:28](=[CH:29][CH:30]=1)[CH2:27][NH:26][CH2:25]2.C(Cl)CCl.[CH:35]1[CH:36]=[CH:37][C:38]2N(O)N=N[C:39]=2[CH:40]=1.CN([CH:48]=[O:49])C>>[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:49][CH2:48][C:39]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:40]=2)[C:15]([C:18]([CH3:20])=[CH2:19])=[CH:14][C:10]=1[C:11]([N:26]1[CH2:25][C:24]2[C:28](=[CH:29][CH:30]=[C:22]([Br:21])[CH:23]=2)[CH2:27]1)=[O:13])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

6

Procedure

A solution of benzyloxy-5-isopropenyl-benzoic acid (2.85 g; 7.6 mmol), 5-bromo-2,3-dihydro-1H-isoindole (1.5 g; 1 equiv.). EDC (1.75 g; 1.2 equiv.) and HOBt (1.25 g; 1.2 equiv.) in DMF (25 ml) was stirred at room temperature overnight then evaporated. The residue was dissolved in EtOAc, washed with 2M HCl then saturated NaHCO3, dried (MgSO4) and evaporated. Purification using a Biotage SP4 (40S, 40 ml/min) eluting with 1:4-1:3-1:2 EtOAc/P.E. gave 2.45 g of (2,4-bis-benzyloxy-5-isopropenyl-phenyl)-(5-bromo-1,3-dihydro-isoindol-2-yl)-methanone as a light brown solid.

Workup

  1. customthen evaporated
  2. dissolutionThe residue was dissolved in EtOAc
  3. washwashed with 2M HCl
  4. dry with materialsaturated NaHCO3, dried (MgSO4)
  5. customevaporated
  6. customPurification
  7. washeluting with 1:4-1:3-1:2 EtOAc/P.E

Sources & evidence

ORD record
ord-08708173ff4d406cb07037ed2ae63cae
Source dataset
uspto-grants-2010_04
Patent number
US07700625B2

Reaction notes

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