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5,5-Diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester → 5,5-Diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid

HRID 1924815
Notes
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Reaction equation

HRID 1924815 reaction equation
C([O:3][C:4]([C:6]1[S:7][CH:8]=[C:9]2[CH2:14][C:13]([CH2:17][CH3:18])([CH2:15][CH3:16])[CH2:12][CH2:11][C:10]=12)=[O:5])C>CCO.[Li+].[OH-].[OH-].[Na+]>[CH2:17]([C:13]1([CH2:15][CH3:16])[CH2:12][CH2:11][C:10]2=[C:6]([C:4]([OH:5])=[O:3])[S:7][CH:8]=[C:9]2[CH2:14]1)[CH3:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 1

HCID 575088905,5-Diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester

Product 1

HCID 575088915,5-Diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acidYield 23%

Reagents, catalysts & solvents 3

HCID 702EthanolSolventHCID 3939Lithium HydroxideSolventHCID 14798Sodium Hydroxide
Solvent

Procedure

A solution of 5,5-diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid ethyl ester (14.2 g, 53.38 mmol) in EtOH (250 mL) and 2 N aq. LiOH (250 mL) is stirred at 65° C. for 18 h. The mixture is diluted with 1 N aq. NaOH and extracted with Et2O. The aq. phase is acidified to pH 2 with 2 N aq. HCl and extracted with DCM. The combined DCM extracts are dried over Na2SO4, filtered, and the solvent is removed in vacuo. The crude product (11.3 g) is purified by MPLC on RP-C18 silica gel to give 5,5-diethyl-4,5,6,7-tetrahydro-benzo[c]thiophene-1-carboxylic acid (2.93 g) as a brown oil; LC-MS: tR=1.01 min, [M+1+CH3CN]=280.19; 1H NMR (CDCl3): δ 7.12 (s, 1H), 2.99 (t, J=7.0 Hz, 2H), 2.46 (s, 2H), 1.59 (t, J=7.0 Hz, 2H), 1.40-1.20 (m, 4H), 0.84-0.74 (m, 6H).

Workup

  1. extractionextracted with Et2O
  2. extractionextracted with DCM
  3. dry with materialThe combined DCM extracts are dried over Na2SO4
  4. filtrationfiltered
  5. customthe solvent is removed in vacuo
  6. customThe crude product (11.3 g) is purified by MPLC on RP-C18 silica gel

Sources & evidence

ORD record
ord-c73766f7eaf44047bcfa611f4def389b
Source dataset
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08178562B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes