HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Acetyl chloride → HCID 86605497, compound

HRID 2103056
Notes
Print preview

Reaction equation

HRID 2103056 reaction equation
[CH2:1]([C:3]1[CH:8]=[C:7]([OH:9])[CH:6]=[C:5]([CH:10]([CH3:12])[CH3:11])[C:4]=1[OH:13])[CH3:2].[C:14](Cl)(=[O:16])[CH3:15].C(N(CC)CC)C.CCCCCC.[CH3:31][CH2:32][O:33]C(C)=O>ClCCl>[C:14]([O:13][C:4]1[C:5]([CH:10]([CH3:12])[CH3:11])=[CH:6][C:7]([O:9][C:32](=[O:33])[CH3:31])=[CH:8][C:3]=1[CH2:1][CH3:2])(=[O:16])[CH3:15]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 6367Acetyl chlorideHCID 8471TriethylamineHCID 21226206Ethyl acetate hexaneHCID 69060363HCID 69060363, compound

Product 1

HCID 86605497HCID 86605497, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of K2S2O8 (8.2 g) in 80 mL of water, was added at once a solution of the above 2-ethyl-6-isopropylphenol (2 g, 12.2 mmol in 25 mL 5% NaOH solution). The mixture was stirred for 3 h and extracted with hexane (3×60 mL). The organic extract was stirred with Na2S2SO4 solution (8.5 g, in 100 mL water) for one hour and the layers were separated. The organic layer was dried over Na2S2O4 and concentrated and dried under high vacuum to give 2-ethyl-6-isopropylbenzene-1,4-diol. To a solution of the crude 2-ethyl-6-isopropylbenzene-1,4-diol in dichloromethane (50 mL) was added acetyl chloride (2.9 g, 36 mmol) and then triethylamine (6 g, 60 mmol) slowly at 0° C. The mixture was stirred at room temperature for 2 h and diluted with hexane/EtOAc (4:1). The mixture was filtered and the filtrate was washed with water (3×80 mL) and dried over Na2SO4 and concentrated. The crude product was purified to afford 2-ethyl-6-isopropyl-1,4-phenylene diacetate as a yellow oil (750 mg).

Workup

  1. customslowly at 0° C
  2. filtrationThe mixture was filtered
  3. washthe filtrate was washed with water (3×80 mL)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customThe crude product was purified

Sources & evidence

ORD record
ord-8644a02927ab4c2db6f45e50c57e66a2
Source dataset
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07576094B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes