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1,4-Benzenedimethanol → 1,2-Benzenedimethanol

HRID 525639
Notes
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Reaction equation

HRID 525639 reaction equation
[C:1]1(CO)[CH:6]=[CH:5][C:4]([CH2:7][OH:8])=[CH:3][CH:2]=1.C(O)(=O)CC[C:14](C)=[O:15].C(N=C=NC(C)C)(C)C>CN(C1C=CN=CC=1)C.ClCCl>[C:3]1([CH2:14][OH:15])[C:4]([CH2:7][OH:8])=[CH:5][CH:6]=[CH:1][CH:2]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 115061,4-BenzenedimethanolHCID 11579Levulinic AcidHCID 12734Diisopropylcarbodiimide

Product 1

HCID 691531,2-BenzenedimethanolYield 191%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6344
Dichloromethane
Solvent

Procedure

In a flask with dichloromethane (ca. 25 ml), 1,4-phenylenedimethanol (5 g, 0.036 mol) and levulinic acid (8.36 g, 0.072 mol) were mixed. The flask was then cooled in an ice water bath. Diisopropyl carbodiimide (9.09 g, 0.072 mol) and the catalyst DMAP (ca. 100 mg) were then added slowly to the solution. The mixture was allowed to come to room temperature and was stirred overnight. The mixture was then filtered and washed with 1M HCL brine. It was then dried over MgSO4 and concentrated in vacuo to afford a white solid as the product (9.5 g). Its purity was ascertained using 1H NMR (300 MHZ in CDCL3): δ 7.34 (s, 4H), 5.11 (s, 4H), 2.77 (t, 4H), 2.62 (t, 4H), 2.18 (s, 6H).

Workup

  1. temperatureThe flask was then cooled in an ice water bath
  2. customto come to room temperature
  3. filtrationThe mixture was then filtered
  4. washwashed with 1M HCL brine
  5. dry with materialIt was then dried over MgSO4
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-8f81c57c43cd473db1297008907b262d
Source dataset
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09340658B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes