Ethyl 4-[(7,8-dihydro-8,8-dimethyl-5-(2-thienyl)naphth-3-yl)ethynyl]benzoate → 4-[(5,6-Dihydro-5,5-dimethyl-8-(2-thienyl)-2-naphthalenyl)ethynyl]benzoic acid

HRID 2393867Notes

Reaction equation

HRID 2393867 reaction equation
CC1(C)C2C=CC(C#CC3C=CC(C(O)=O)=CC=3)=CC=2C(C#CCCC)=CC1.[CH3:29][C:30]1([CH3:58])[C:39]2[CH:38]=[CH:37][C:36]([C:40]#[C:41][C:42]3[CH:52]=[CH:51][C:45]([C:46]([O:48]CC)=[O:47])=[CH:44][CH:43]=3)=[CH:35][C:34]=2[C:33]([C:53]2[S:54][CH:55]=[CH:56][CH:57]=2)=[CH:32][CH2:31]1>>[CH3:29][C:30]1([CH3:58])[C:39]2[CH:38]=[CH:37][C:36]([C:40]#[C:41][C:42]3[CH:43]=[CH:44][C:45]([C:46]([OH:48])=[O:47])=[CH:51][CH:52]=3)=[CH:35][C:34]=2[C:33]([C:53]2[S:54][CH:55]=[CH:56][CH:57]=2)=[CH:32][CH2:31]1

Participants

3

Procedure

Employing the same general procedure as for the preparation of 4-[(7,8-dihydro-8,8-dimethyl-5-(1-pentynyl)naphth-2-yl)ethynyl]benzoic acid (Compound 84), 70.0 mg (0.17 mmol) of ethyl 4-[(7,8-dihydro-8,8-dimethyl-5-(2-thienyl)naphth-3-yl)ethynyl]benzoate (Compound 123) was converted into the title compound (colorless solid) using 17.8 mg (0.42 mmol) of LiOH in H2O.

Sources & evidence

ORD record
ord-ea56456cc17f4b35ad0a63fb06c43552
Source dataset
uspto-grants-1998_09
Patent number
US05808083

Reaction notes

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