HCID 178442822, compound → HCID 178442824, compound

HRID 483664Notes

Reaction equation

HRID 483664 reaction equation
[CH:1]([C:13]1[C:14](=[O:25])[C:15]2[C:20]([C:21](=[O:24])[C:22]=1[OH:23])=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].OC1C(=O)C2C(C(=O)C=1)=CC=CC=2>>[C:21]1(=[O:24])[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[C:14](=[O:25])[CH:13]=[CH:22]1.[CH:1]([C:13]1[C:14](=[O:25])[C:15]2[C:20]([C:21](=[O:24])[C:22]=1[OH:23])=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

3

Reactant 2

HCID 178442822HCID 178442822, compoundHCID 178516607HCID 178516607, compound

Product 1

HCID 178442824HCID 178442824, compound

Procedure

Thus, by this reaction, 2-(1-dodecenyl)-3-hydroxy-1,4-naphthoquinone was prepared from 2-hydroxy-1,4-naphthoquinone in a yield of 93.3 mol %.

Sources & evidence

ORD record
ord-ec6b060c6c264145944af78b365e680e
Source dataset
uspto-grants-1993_07
Patent number
US05225578

Reaction notes

Loading…