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Acetyl chloride → 9-Acetyl-1,2-dihydrocyclopenta[c]carbazol-3(6H)-one

HRID 1615037
Notes
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Reaction equation

HRID 1615037 reaction equation
[CH2:1]1[C:16]2[C:15]3[C:14]4[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=4[NH:8][C:7]=3[CH:6]=[CH:5][C:4]=2[C:3](=[O:17])[CH2:2]1.[Al+3].[Cl-].[Cl-].[Cl-].[C:22](Cl)([CH3:24])=[O:23]>C(Cl)Cl>[C:22]([C:12]1[CH:11]=[CH:10][C:9]2[NH:8][C:7]3[CH:6]=[CH:5][C:4]4[C:3](=[O:17])[CH2:2][CH2:1][C:16]=4[C:15]=3[C:14]=2[CH:13]=1)(=[O:23])[CH3:24]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6367Acetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 585448961,6-Dihydrocyclopenta[c]carbazol-3(2H)-one

Product 1

HCID 585448999-Acetyl-1,2-dihydrocyclopenta[c]carbazol-3(6H)-oneYield 56.3%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

1,2-dihydro-6H-cyclopenta[c]carbazole-3-one 90 (6 g, 27.1 mmol) was suspended in dry CH2Cl2 (100 mL). Anhydrous AlCl3 (6 g, 45 mmol) was added with stirring on ice bath, followed by the dropwise addition of AcCl (2.4 mL, 33.2 mmol). The reaction mixture was stirred at about 5° C. for 24 h, and poured into ice water. The precipitated grey solid was filtered off, washed with water (2×100 mL), acetone (3×50 mL), diethyl ether (3×50 mL) to give 4 g (56.3%) of 9-acetyl-1,2-dihydro-6H-cyclopenta[c]carbazole-3-one 91.

Workup

  1. stirringThe reaction mixture was stirred at about 5° C. for 24 h
  2. filtrationThe precipitated grey solid was filtered off
  3. washwashed with water (2×100 mL), acetone (3×50 mL), diethyl ether (3×50 mL)

Sources & evidence

ORD record
ord-d53f780ace724920a21c3c49f2a963d6
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08765738B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes