Water → Methyl 4-allyl-3-(4-benzyloxyazepan-1-yl)sulfonyl-benzoate

HRID 713161Notes

Reaction equation

HRID 713161 reaction equation
[CH2:1]([O:8][CH:9]1[CH2:15][CH2:14][CH2:13][N:12]([S:16]([C:19]2[CH:20]=[C:21]([CH:26]=[CH:27][C:28]=2Br)[C:22]([O:24][CH3:25])=[O:23])(=[O:18])=[O:17])[CH2:11][CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:30]([Sn](CCCC)(CCCC)CCCC)[CH:31]=[CH2:32].CCOC(C)=O.O>C1(C)C=CC=CC=1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:32]([C:28]1[CH:27]=[CH:26][C:21]([C:22]([O:24][CH3:25])=[O:23])=[CH:20][C:19]=1[S:16]([N:12]1[CH2:13][CH2:14][CH2:15][CH:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:10][CH2:11]1)(=[O:18])=[O:17])[CH:31]=[CH2:30]

Participants

7

Reactant 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 90628AllyltributylstannaneHCID 118222070methyl 3-(4-benzyloxyazepan-1-yl)Sulfonyl-4-bromo-benzoate

Product 1

HCID 118222059Methyl 4-allyl-3-(4-benzyloxyazepan-1-yl)sulfonyl-benzoateYield 52.8%

Reagents, catalysts & solvents 2

HCID 178418397HCID 178418397, compoundCatalystHCID 1140TolueneSolvent

Conditions

Temperature
110 °C

Procedure

Methyl 3-(4-benzyloxyazepan-1-yl)sulfonyl-4-bromo-benzoate (1.30 g, 2.69 mmol, 1.00 Eq), allyl(tributyl)stannane (1.07 g, 3.23 mmol, 1.20 Eq) LiCl (136.83 mg, 3.23 mmol, 1.20 Eq) and Pd(PPh3)4 (310.85 mg, 269.00 umol, 0.10 Eq) in TOLUENE (20 mL) was de-gassed and then heated to 110° C. for 16 hr under N2. TLC (PE:EtOAc=1:1) showed the starting material and the product was the same spot. The reaction mixture was poured into H2O, extracted with EA. The organic phase was dried over anhydrous Na2SO4, concentrated in vacuum to give a residue, which was purified by column chromatography (silica gel, eluting with PE:EA=1:1) to afford the pure methyl 4-allyl-3-(4-benzyloxyazepan-1-yl)sulfonyl-benzoate (630.00 mg, 1.42 mmol, 52.80% yield) as light yellow solid.

Workup

  1. extractionextracted with EA
  2. dry with materialThe organic phase was dried over anhydrous Na2SO4
  3. concentrationconcentrated in vacuum
  4. customto give a residue, which
  5. customwas purified by column chromatography (silica gel, eluting with PE:EA=1:1)

Sources & evidence

ORD record
ord-a51705e809d64e1095bdda39f7d419ea
Source dataset
uspto-grants-2015_11
Patent number
US09181288B2

Reaction notes

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