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Methacrylic Acid → (2-Adamantyloxymethyl)methacrylate

HRID 504976
Notes
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Reaction equation

HRID 504976 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].C(N(CC)CC)C.Cl[CH2:15][O:16][CH:17]1[CH:24]2[CH2:25][CH:20]3[CH2:21][CH:22]([CH2:26][CH:18]1[CH2:19]3)[CH2:23]2>O1CCCC1>[CH:18]12[CH2:26][CH:22]3[CH2:21][CH:20]([CH2:25][CH:24]([CH2:23]3)[CH:17]1[O:16][CH2:15][O:5][C:1](=[O:6])[C:2]([CH3:4])=[CH2:3])[CH2:19]2
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 4093Methacrylic AcidHCID 8471TriethylamineHCID 10932491HCID 10932491, compound

Product 1

HCID 23150858(2-Adamantyloxymethyl)methacrylate

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Procedure

6.9 g of methacrylic acid was dissolved in 200 ml of tetrahydrofuran, and 8.0 g of triethylamine was added. Following stirring at room temperature, a solution containing 15 g of 2-adamantyl chloromethyl ether dissolved in 100 ml of tetrahydrofuran was added dropwise to the reaction solution. Following stirring for 12 hours at room temperature, the precipitated salt was removed by filtration. The solvent was removed from the remaining filtrate by evaporation, the residue was dissolved in 200 ml of ethyl acetate, and following washing with pure water (100 ml×3), the solvent was removed by evaporation. The residue was then allowed to stand under ice cooling, thereby yielding a white solid.

Workup

  1. additionwas added dropwise to the reaction solution
  2. stirringFollowing stirring for 12 hours at room temperature
  3. customthe precipitated salt was removed by filtration
  4. customThe solvent was removed from the remaining filtrate by evaporation
  5. dissolutionthe residue was dissolved in 200 ml of ethyl acetate
  6. washfollowing washing with pure water (100 ml×3)
  7. customthe solvent was removed by evaporation
  8. customyielding a white solid

Sources & evidence

ORD record
ord-eb6ffdde59ca4436b863364d9976cb37
Source dataset
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07781144B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes