Stearyl Alcohol → Octadecyl o-iodobenzoate

HRID 894498

Reaction equation

[I:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](Cl)=[O:5].[CH2:11]([OH:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]>>[I:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([O:29][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[O:5]

Participants

Reactant 2

HCID 8221Stearyl Alcohol

HCID 691122-Iodobenzoyl chloride

Product 1

HCID 12945188Octadecyl o-iodobenzoate

Procedure

One ml of o-iodobenzoyl chloride was reacted with 2.7 g of 1-octadecanol in accordance with the procedure of Example 8. There was obtained 2.36 g of octadecyl o-iodobenzoate, mp 35°, Rf 0.66.

Sources & evidence

ORD record: ord-4450edcf49c943c98c75325fb948d949
Source dataset: uspto-grants-1981_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04284619

Linked notes

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