Lithium Hydroxide → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid
Reaction equation
O(CCSCC1C=CC(C2C=CC=C(C(O)=O)C=2)=CC=1)C1C=CC=CC=1.C([O:29][C:30]([C:32]1[C:33]([C:38]2[CH:43]=[CH:42][CH:41]=[C:40]([CH2:44][S:45][CH2:46][CH2:47][O:48][C:49]3[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=3)[CH:39]=2)=[CH:34][CH:35]=[CH:36][CH:37]=1)=[O:31])C.[OH-].[Li+]>C1COCC1>[O:48]([CH2:47][CH2:46][S:45][CH2:44][C:40]1[CH:39]=[C:38]([C:33]2[C:32]([C:30]([OH:31])=[O:29])=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH:43]=[CH:42][CH:41]=1)[C:49]1[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid was synthesized as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid. 3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid ethyl ester (2.1 g, 5.35 mmol, 1 eq.) in 30% aqueous THF was treated with lithium hydroxide (0.38 g, 16.05 mmol, 3 eq.). When complete, the reaction was worked up as described leaving 3′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (1.94, 99% yield) as a yellow oil.
Workup
- custom3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid was synthesized
Sources & evidence
- ORD record
- ord-f065fc5672104e7cb34ce0cb6157b0cf
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132456B2
Reaction notes
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