Oxalyl chloride → 7-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one

HRID 2242600Notes

Reaction equation

HRID 2242600 reaction equation
[C:1]1([S:7][C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH2:16][C:17]([OH:19])=O)=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(Cl)(=O)C(Cl)=O.[Cl-].[Cl-].[Cl-].[Al+3]>O1CCCC1.CN(C=O)C>[C:1]1([S:7][C:8]2[CH:9]=[C:10]3[C:11]([CH2:14][CH2:15][CH2:16][C:17]3=[O:19])=[CH:12][CH:13]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Reactant 3

HCID 65578Oxalyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 248345484-[4-(Phenylsulfanyl)phenyl]butanoic acid

Product 1

HCID 590217307-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-oneYield 55.5%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideCatalystHCID 8028TetrahydrofuranSolvent

Procedure

4-(4-Phenylsulfanyl-phenyl)-butyric acid (5.0 g, 18.4 mmol) was dissolved in 50 mL tetrahydrofuran (THF). Oxalyl chloride (1.8 mL, 20 mmol) and one drop of DMF were added, and the reaction mixture was stirred for 1 hour, and then evaporated to dryness under reduced pressure. The resulting residue was dissolved in 40 mL of 1,2-dichloroethane, and aluminum trichloride (0.85 g, 25 mmol) was added all at once. The reaction mixture was stirred for 1 hour, and quenched by addition of 2% HCl. This aqueous mixture was extracted twice with 100 mL of EtOAc, and the combined organic layers were dried (MgSO4) and evaporated to yield 2.54 g (10 mmol, 55.5%) of 7-phenylsulfanyl-3,4-dihydro-2H-naphthalen-1-one as a gummy residue. MS: 255 (M+H)+.

Workup

  1. customevaporated to dryness under reduced pressure
  2. dissolutionThe resulting residue was dissolved in 40 mL of 1,2-dichloroethane
  3. stirringThe reaction mixture was stirred for 1 hour
  4. customquenched by addition of 2% HCl
  5. extractionThis aqueous mixture was extracted twice with 100 mL of EtOAc
  6. dry with materialthe combined organic layers were dried (MgSO4)
  7. customevaporated

Sources & evidence

ORD record
ord-928962dc452c4a51bf8c9545d60b74f5
Source dataset
uspto-grants-2010_03
Patent number
US07671235B2

Reaction notes

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