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3,3-Dimethyl-1-butyne → HCID 86700848, compound

HRID 881746
Notes
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Reaction equation

HRID 881746 reaction equation
[CH2:1]([O:3][C:4]([C:6]1([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:11][CH2:10][C:9](OS(C(F)(F)F)(=O)=O)=[CH:8][CH2:7]1)=[O:5])[CH3:2].[Cl:25][C:26]1[CH:31]=[CH:30][C:29](OB(O)O)=[CH:28][CH:27]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].C(C#C)(C)(C)C>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl.C(COC)OC.C(O)C>[CH2:1]([O:3][C:4]([C:6]1([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:11][CH2:10][C:9]([C:29]2[CH:30]=[CH:31][C:26]([Cl:25])=[CH:27][CH:28]=2)=[CH:8][CH2:7]1)=[O:5])[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 135123,3-Dimethyl-1-butyneHCID 62657Potassium Phosphate, TribasicHCID 17810664p-Chlorophenylboric acidHCID 86692328HCID 86692328, compound

Product 1

HCID 86700848HCID 86700848, compoundYield 76.4%

Reagents, catalysts & solvents 3

HCID 178418807
HCID 178418807, compound
Catalyst
HCID 702EthanolSolvent
HCID 80711,2-DimethoxyethaneSolvent

Conditions

Temperature
80 °C

Procedure

A 100 ml heavy wall round bottom flask was charged with the crude intermediate 4-trifluoromethanesulfonyloxy-cyclohex-3-ene-1,1-dicarboxylic acid diethyl ester (4.0 g, 80% purity, 8.55 mmol, 1.0 equiv) from last step, PdCl2(dppf)-CH2Cl2 adduct (0.628 g, 0.769 mmol, 0.09 equiv), 4-chloro-phenylboric acid (2.67 g, 17.1 mmol, 2.0 equiv), tripotassium phosphate (4.54 g, 21.37 mmol, 2.5 equiv), ethanol (8 ml), dimethoxyethane (32.0 ml) and t-butyl acetylene (7.9 g, 97 mmol, 2.0 equiv). The flask was sealed, flushed with nitrogen for three times and stirred at 80° C. for 16 hours. After cooled at room temperature, the reaction mixture was filtered and washed with ethyl acetate (20 ml). The filtrate was concentrated under vacuum and the residue was purified by chromatography (heptanes/ethyl acetate 2/1) to give 4-(4-chloro-phenyl)-cyclohex-3-ene-1,1-dicarboxylic acid diethyl ester (2.2 g, 76%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.27 (t, J=8.00 Hz, 6H) 2.29 (t, J=6.38 Hz, 2H) 2.46 (td, J=6.25, 2.02 Hz, 2H) 2.65-2.85 (m, 2H) 4.21 (q, J=8.00 Hz, 4H) 6.07 (m, 1H) 7.26 (s, 4H).

Workup

  1. customThe flask was sealed
  2. customflushed with nitrogen for three times
  3. temperatureAfter cooled at room temperature
  4. filtrationthe reaction mixture was filtered
  5. washwashed with ethyl acetate (20 ml)
  6. concentrationThe filtrate was concentrated under vacuum
  7. customthe residue was purified by chromatography (heptanes/ethyl acetate 2/1)

Sources & evidence

ORD record
ord-03299d46a4994367b580144cf7b2b9c1
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08993619B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes