Lithium Hydroxide → 3'-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid

HRID 719712Notes

Reaction equation

HRID 719712 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[CH:37]=[CH:36][C:35]([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:33]=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:35]2[CH:34]=[CH:33][C:32]([C:30]([OH:31])=[O:29])=[CH:37][CH:36]=2)[CH:43]=[CH:42][CH:41]=1)[C:49]1[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1

Participants

5

Procedure

3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid was synthesized as described for 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-3-carboxylic acid. 3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid ethyl ester (2.0 g, 5.1 mmol, 1 eq.) in 30% aqueous THF was treated with lithium hydroxide (0.37 g, 15.3 mmol, 3 eq.). When complete, the reaction was worked up as described leaving 3′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid (1.68 g, 90% yield) as a white solid.

Workup

  1. custom3′-(2-Phenoxy-ethylsulfanylmethyl)-biphenyl-4-carboxylic acid was synthesized

Sources & evidence

ORD record
ord-1098ecdda0754e519f3f60133e161a81
Source dataset
uspto-grants-2006_11
Patent number
US07132456B2

Reaction notes

Loading…