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Benzyl Alcohol → HCID 69358566, compound

HRID 852546
Notes
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Reaction equation

HRID 852546 reaction equation
CC[N:3]([CH2:6][CH3:7])[CH2:4]C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:15])C=CC=CC=1.[CH3:25][O:26][C:27](=[O:40])[C:28]1[CH:36]=[C:35]([O:37][CH2:38][CH3:39])C=C(C(O)=O)[CH:29]=1.[CH2:41]([OH:48])[C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1>C1(C)C=CC=CC=1>[CH3:25][O:26][C:27](=[O:40])[C:28]1[CH:36]=[C:35]([O:37][CH2:38][CH3:39])[CH:7]=[C:6]([NH:3][C:4]([O:48][CH2:41][C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=2)=[O:15])[CH:29]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 244Benzyl AlcoholHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 69357330HCID 69357330, compound

Product 1

HCID 69358566HCID 69358566, compoundYield 62%

Reagents, catalysts & solvents 1

HCID 1140
Toluene
Solvent

Conditions

Temperature
80 °C

Procedure

NEt3 (14.2 ml, 102 mmol, 1.3 equiv) and diphenylphosphoryl azide (22 ml, 102 mmol, 1.3 equiv) were added to a suspension of 5-ethoxy-isophthalic acid monomethyl ester (D45) (17.6 g, 78.6 mmol, 1 equiv) in toluene (250 ml) and the mixture heated at 80° C. for 3 h. Benzyl alcohol (12 ml, 118 mmol, 1.5 equiv) was added and the resulting mixture was refluxed for 4 h, cooled to room temperature and concentrated in vacuo. The residue was dissolved in AcOEt (300 ml) and the resulting solution was washed with 2N aqueous HCl solution (100 ml) followed by saturated aqueous NaHCO3 solution (100 ml), dried over MgSO4 and concentrated in vacuo. The residue was triturated with Et2O to give 3-benzyloxycarbonylamino-5-ethoxy-benzoic acid methyl ester (D47) (15 g, 62%) as a white solid. [M−H]−=328.1, RT=3.46 min

Workup

  1. temperaturethe resulting mixture was refluxed for 4 h
  2. temperaturecooled to room temperature
  3. concentrationconcentrated in vacuo
  4. dissolutionThe residue was dissolved in AcOEt (300 ml)
  5. washthe resulting solution was washed with 2N aqueous HCl solution (100 ml)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo
  8. customThe residue was triturated with Et2O

Sources & evidence

ORD record
ord-e17097be26e84116ab66079d68cb3044
Source dataset
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07253198B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes