1-Chlorooctane → HCID 86688831, compound

HRID 2275521Notes

Reaction equation

[C:1]([OH:6])(=[O:5])[CH2:2][CH2:3][CH3:4].[C:7]([O:23][CH2:24][CH3:25])(=[O:22])[CH2:8][C:9]([CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])([C:11]([O:13][CH2:14][CH3:15])=[O:12])[OH:10].C(Cl)CCCCCCC>>[C:1]([OH:6])(=[O:5])[CH2:2][CH2:3][CH2:4][CH2:7][CH2:8][CH2:9][CH3:11].[C:17]([O:19][CH2:20][CH3:21])(=[O:18])[CH2:16][C:9]([CH2:8][C:7]([O:23][CH2:24][CH3:25])=[O:22])([C:11]([O:13][CH2:14][CH3:15])=[O:12])[OH:10]

Participants

Reactant 2

HCID 81421-Chlorooctane

HCID 86688830HCID 86688830, compound

Product 1

HCID 86688831HCID 86688831, compound

Procedure

The same procedure was used as for preparation of triethyl citrate butyrate but using octyl chloride.

Sources & evidence

ORD record: ord-1a8efb90262e4f12965ba87e1b347e95
Source dataset: uspto-grants-2015_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US09127232B2

Reaction notes

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