ethyl 3,3-bis(4-fluorophenyl)-2-[2-triphenylmethyl-2H-tetrazol-5-yl]-2-propenoate → HCID 14724008, compound

HRID 1195385Notes

Reaction equation

HRID 1195385 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:39]2[CH:44]=[CH:43][C:42]([F:45])=[CH:41][CH:40]=2)=[C:9]([C:15]2[N:16]=[N:17][N:18]([C:20]([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[N:19]=2)[C:10](OCC)=[O:11])=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C>C(Cl)Cl>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([C:39]2[CH:44]=[CH:43][C:42]([F:45])=[CH:41][CH:40]=2)=[C:9]([C:15]2[N:16]=[N:17][N:18]([C:20]([C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)[C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[N:19]=2)[CH2:10][OH:11])=[CH:6][CH:7]=1

Participants

4

Procedure

To a stirred solution of 3 g (5 mmol) ethyl 3,3-bis(4-fluorophenyl)-2-[2-triphenylmethyl-2H-tetrazol-5-yl]-2-propenoate in 50 mL of methylene chloride at -70° C., 10 mL (15 mmol) diisobutylaluminium hydride solution (1.5M in methylene chloride) was added and the solution stirred for 3 hours. The reaction was quenched with water and the mixture extracted with methylene chloride. The combined organic fractions were dried with magnesium sulfate and concentrated in vacuo to give 2.1 g of the title compound; m.p.=176°-178° C.

Workup

  1. customThe reaction was quenched with water
  2. extractionthe mixture extracted with methylene chloride
  3. dry with materialThe combined organic fractions were dried with magnesium sulfate
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-bb53c77c338e437a9bc327dad752e130
Source dataset
uspto-grants-1992_05
Patent number
US05110940

Reaction notes

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