2-Chloro-5-methylphenol → HCID 71075549, compound

HRID 2170693Notes

Reaction equation

HRID 2170693 reaction equation
[OH:1][C@@H:2]([CH:7]([CH3:9])[CH3:8])[C:3]([O:5][CH3:6])=[O:4].[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][C:12]=1O>>[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([CH3:17])=[CH:13][C:12]=1[O:1][C@H:2]([CH:7]([CH3:9])[CH3:8])[C:3]([O:5][CH3:6])=[O:4]

Participants

3

Reactant 2

HCID 120082-Chloro-5-methylphenolHCID 11194352Methyl (2S)-2-hydroxy-3-methylbutanoate

Product 1

HCID 71075549HCID 71075549, compound

Procedure

The title compound was prepared following the same protocol as described in Step 1, Example 42, using the (S)-methyl 2-hydroxy-3-methylbutanoate instead of the (S)-methyl 2-hydroxypropanoate and the 2-chloro-5-methylphenol instead of the m-cresol.

Sources & evidence

ORD record
ord-df339de9a7b847789dc6394c927f0f3f
Source dataset
uspto-grants-2015_06
Patent number
US09051265B2

Reaction notes

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