Triethylamine → Methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate

HRID 14292

Reaction equation

HRID 14292 reaction equation
[I:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([O:13][CH3:14])=[O:12])[CH:10]=1)[C:5]([OH:7])=O.C(N(CC)CC)C.[CH2:22]([NH:25][CH2:26][CH2:27][CH3:28])[CH2:23][CH3:24].[I-].ClC1C=CC=C[N+]=1C>C(Cl)Cl>[CH2:22]([N:25]([CH2:26][CH2:27][CH3:28])[C:5]([C:4]1[CH:8]=[C:9]([CH:10]=[C:2]([I:1])[CH:3]=1)[C:11]([O:13][CH3:14])=[O:12])=[O:7])[CH2:23][CH3:24]

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 8902DipropylamineHCID 1670692-Chloro-1-methylpyridinium iodideHCID 158403913-Iodo-5-(methoxycarbonyl)benzoic acid

Product 1

HCID 21086179Methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoateYield 79.8%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a mixture of 3-iodo-5-(methoxycarbonyl)benzoic acid (65.8 g, 0.215 mol), triethylamine (52.2 g, 0.516 mol), and dipropylamine (23.9 g, 0.237 mol) in methylene chloride (950 mL) was added 2-chloro-1-methylpyridinium iodide (65.9 g, 0.258 mol). The reaction mixture was stirred at room temperature for 15 h and then concentrated under reduced pressure. Purification by silica gel plug (3:1 hexanes/ethyl acetate) provided methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate (66.8 g): 1NMR (300 MHz, CDCl3) δ 8.39 (s, 1H), 7.98 (s, 1H), 7.88 (s, 1H), 3.93 (s, 3H), 3.45 (m, 2H), 3.14 (m, 2H), 1.69 (m, 2H), 1.54 (m, 2H), 0.98 (m, 3H), 0.77 (m, 3H).

Workup

  1. concentrationconcentrated under reduced pressure
  2. customPurification by silica gel plug (3:1 hexanes/ethyl acetate)

Sources & evidence

ORD record
ord-3ff1d7eb3b374b1b819b39c831cf1ff1
Source dataset
uspto-grants-2010_06
Patent number
US07727997B2

Linked notes

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