Chloroacetyl chloride → HCID 20315558, compound

HRID 2419370Notes

Reaction equation

HRID 2419370 reaction equation
[O:1]([CH:8]([CH3:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:15][CH2:16][C:17](Cl)=[O:18].C(N(CC)C(=O)COC1C=CC(C(=O)CCl)=CC=1)C>>[Cl:15][CH2:16][C:17]([C:5]1[CH:6]=[CH:7][C:2]([O:1][CH:8]([CH3:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[CH:3][CH:4]=1)=[O:18]

Participants

4

Reactant 3

HCID 6577Chloroacetyl chlorideHCID 4496358HCID 4496358, compoundHCID 20315556HCID 20315556, compound

Product 1

HCID 20315558HCID 20315558, compound

Procedure

Ethyl 2-phenoxypropionate was reacted with chloroacetyl chloride as described for N,N-diethyl-4-(chloroacetyl)phenoxyacetamide, used as a starting material for Example 7, to give ethyl 2-[4-(chloroacetyl)phenoxy]-propionate as a white solid, having a satisfactory analysis (found: C, 57.7, H, 5.5, N, 13.0; required: C, 57.7; H, 5.6; N, 13.1).

Sources & evidence

ORD record
ord-c0a15354474c41479d9b086d2568a208
Source dataset
uspto-grants-1978_08
Patent number
US04105790

Reaction notes

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