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
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]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 3
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
- extractionextracted with Et2O
- extractionextracted with DCM
- dry with materialThe combined DCM extracts are dried over Na2SO4
- filtrationfiltered
- customthe solvent is removed in vacuo
- customThe crude product (11.3 g) is purified by MPLC on RP—C18 silica gel
Sources & evidence
- ORD record
- ord-05be8c729a13414a808a49b8e57d662a
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08697732B2
Reaction notes
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