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Formaldehyde → Ethyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate

HRID 606584
Notes
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Reaction equation

HRID 606584 reaction equation
[CH3:1][C:2]1[C:6]2[CH:7]=[C:8]([O:11][CH2:12][CH:13]3[O:18][CH2:17][CH2:16][N:15]([C:19](OC(C)(C)C)=O)[CH2:14]3)[CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:26]([O:28][CH2:29][CH3:30])=[O:27].C=O.O.C([BH3-])#N.[Na+]>Cl.O1CCOCC1>[CH3:1][C:2]1[C:6]2[CH:7]=[C:8]([O:11][CH2:12][CH:13]3[O:18][CH2:17][CH2:16][N:15]([CH3:19])[CH2:14]3)[CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:26]([O:28][CH2:29][CH3:30])=[O:27]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 712FormaldehydeHCID 962WaterHCID 5003444Sodium cyanoborohydrideHCID 67046655ethyl 3-methyl-5-(4-Boc-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate

Product 1

HCID 67046419Ethyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate

Reagents, catalysts & solvents 2

HCID 313
Hydrochloric Acid
Solvent
HCID 312751,4-DioxaneSolvent

Procedure

Ethyl 3-methyl-5-(4-Boc-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate (1.05 mmol) was dissolved in 30 ml of a 4.0 M solution of hydrochloric acid in dioxan and stirred at room temperature for 1 hour. After removing the solvent under vacuo the resulting amine was dissolved in 20 ml of a mixture 2 to 1 of methanol and a buffered solution of acetic acid and sodium acetate at pH=5.3. A 37% solution of formaldehyde in water (1.16 mmol) was added and the mixture was stirred at room temperature for 1 hour. Then sodium cyanoborohydride (1.16 mmol) was added and the mixture was stirred over night at room temperature. The methanol was removed under vacuo and the water was eliminated by liophylisation. The solid obtained was purified by flash chromatography to yield ethyl 3-methyl-5-(4-methyl-morpholin-2-ylmethoxy)-benzofuran-2-carboxylate: m/z=334 in MS ES+, as a white solid.

Workup

  1. customAfter removing the solvent under vacuo the resulting amine
  2. dissolutionwas dissolved in 20 ml of a mixture 2 to 1 of methanol
  3. stirringthe mixture was stirred at room temperature for 1 hour
  4. stirringthe mixture was stirred over night at room temperature
  5. customThe methanol was removed under vacuo
  6. customThe solid obtained
  7. customwas purified by flash chromatography

Sources & evidence

ORD record
ord-7db421f564a64c2590ae67e10d6442cb
Source dataset
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07915300B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes