Aluminiumhydride → HCID 18546174, compound

HRID 1739032Notes

Reaction equation

[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18](/[C:21](/[CH3:27])=[CH:22]/[C:23](OC)=[O:24])=[CH:17][CH:16]=1.[H-].[Al+3].[H-].[H-]>>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)=[N:4][C:3]=1[CH2:13][O:14][C:15]1[CH:16]=[CH:17][C:18](/[C:21](/[CH3:27])=[CH:22]/[CH2:23][OH:24])=[CH:19][CH:20]=1

Participants

Reactant 2

HCID 21584524Aluminiumhydride

HCID 86754595HCID 86754595, compound

Product 1

HCID 18546174HCID 18546174, compoundYield 63%

Procedure

According to the same manner as that described in reference Example 10, methyl (E)-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]-2-butenoate was reduced with sobutyl aluminum hydride to give (E)-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]-2-butenol (yield: 63%). This product was recrystallized from ethyl acetate-ether. colorless crystals, mp: 126-127° C.

Sources & evidence

ORD record: ord-b6140d290cd6490f89298b0d2a3f32ab
Source dataset: uspto-grants-1999_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05965589

Reaction notes

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