Methoxyacetyl chloride → HCID 20453269, compound

HRID 1462457Notes

Reaction equation

HRID 1462457 reaction equation
[CH3:1][C:2]1[CH:14]=[CH:13][CH:12]=[C:11]([CH3:15])[C:3]=1[NH:4][CH:5]1[CH2:10][O:9][C:7](=[O:8])[CH2:6]1.[CH3:16][O:17][CH2:18][C:19](Cl)=[O:20]>>[CH3:16][O:17][CH2:18][C:19]([N:4]([CH:5]1[CH2:10][O:9][C:7](=[O:8])[CH2:6]1)[C:3]1[C:11]([CH3:15])=[CH:12][CH:13]=[CH:14][C:2]=1[CH3:1])=[O:20]

Participants

3

Reactant 2

HCID 96623Methoxyacetyl chlorideHCID 20150686HCID 20150686, compound

Product 1

HCID 20453269HCID 20453269, compound

Procedure

3-(2,6-dimethylanilino)-gamma-butyrolactone was acylated with methoxyacetyl chloride according to the procedure described in Example 2C above to yield N-methoxyacetyl-3-(2,6-dimethylanilino)-gamma-butyrolactone.

Sources & evidence

ORD record
ord-627df14dd7d343e9a522d0cfc32fd1f6
Source dataset
uspto-grants-1984_07
Patent number
US04460603

Reaction notes

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