HCID 21387529, compound → HCID 21387565, compound

HRID 1833859Notes

Reaction equation

HRID 1833859 reaction equation
Cl[C:2]1[CH:15]=[CH:14][CH:13]=[CH:12][C:3]=1[CH:4]([C:7]1[O:8][CH:9]=[CH:10][CH:11]=1)[O:5][CH3:6].[OH:16][CH:17](C1OC=CC=1)C1C=CC=CC=1OC>>[CH3:6][O:5][CH:4]([C:7]1[O:8][CH:9]=[CH:10][CH:11]=1)[C:3]1[CH:12]=[CH:13][CH:14]=[CH:15][C:2]=1[O:16][CH3:17]

Participants

3

Reactant 2

HCID 21387529HCID 21387529, compoundHCID 21387660HCID 21387660, compound

Product 1

HCID 21387565HCID 21387565, compound

Procedure

(±) 2-(α,2-Dimethoxybenzyl)furan (b.p. 112°-115° C./0.1 mm.Hg) was prepared in a manner similar to that described in Example 3(k) for the preparation of (±) 2-(2-chloro-α-methoxybenzyl)furan but replacing the (±) 2-(2-chloro-α-hydroxybenzyl)furan by (±) 2(α-hydroxy-2-methoxybenzyl)furan.

Sources & evidence

ORD record
ord-bdf0a8f693a34fda8ffdd07571ee7b2f
Source dataset
uspto-grants-1978_01
Patent number
US04067723

Reaction notes

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