HCID 18461162, compound → HCID 57857234, compound

HRID 503659Notes

Reaction equation

HRID 503659 reaction equation
[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:15]=[C:14](Cl)[C:10]=1[C:11]([OH:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[C:28]1C(CC)=C(C=C[C:36]=1O)C(O)=O.ClC1C(CC)=C(C=CC=1O)C=O>>[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:15]=[C:14]([CH2:28][CH3:36])[C:10]=1[C:11]([OH:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

4

Reactant 3

HCID 18461162HCID 18461162, compoundHCID 57857235HCID 57857235, compoundHCID 67183044HCID 67183044, compound

Product 1

HCID 57857234HCID 57857234, compound

Procedure

2,4-bisbenzyloxy-6-chlorobenzoic acid, m.p. 135-1360 (35%) and 3-chloro-2-ethyl-4-hydroxybenzoic acid from 3-chloro-2-ethyl-4-hydroxybenzaldehyde: yield 51%, m.p. 138-1390.

Sources & evidence

ORD record
ord-439cf22365734637be67dba460737cfb
Source dataset
uspto-grants-2010_08
Patent number
US07776920B2

Reaction notes

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