HCID 21409403, compound → HCID 54526394, compound

HRID 2072454Notes

Reaction equation

HRID 2072454 reaction equation
C([O:4][CH2:5][C:6]1[CH:11]=[CH:10][C:9]([C:12](=[O:17])[C:13]([CH3:16])([CH3:15])[CH3:14])=[CH:8][C:7]=1[Cl:18])(=O)C.C(OCC1C=CC(C(=O)C(C)(C)C)=CC=1)(=O)C>>[Cl:18][C:7]1[CH:8]=[C:9]([C:12](=[O:17])[C:13]([CH3:15])([CH3:14])[CH3:16])[CH:10]=[CH:11][C:6]=1[CH2:5][OH:4]

Participants

3

Reactant 2

HCID 21409403HCID 21409403, compoundHCID 21409404HCID 21409404, compound

Product 1

HCID 54526394HCID 54526394, compound

Procedure

Following the above procedure, but using an equivalent amount of α-acetoxy-2-chloro-4-pivaloyl-toluene in plce of the α-acetoxy-p-pivaloyl-toluene, there is obtained 2-chloro-4-pivaloyl-benzyl alcohol.

Sources & evidence

ORD record
ord-c0e279d17b7f4f43b74adc3c0df320b1
Source dataset
uspto-grants-1977_09
Patent number
US04051261

Reaction notes

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