Diallyl ether → HCID 19101044, compound

Reaction equation

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

Participants

Reactant 2

HCID 11194Diallyl ether

HCID 18015Hexadecanethiol

Product 1

HCID 19101044HCID 19101044, compound

Procedure

The procedure that is used for this example is similar to that set forth in Example 3, except that n-hexadecyl mercaptan (129.26g., 0.5 mole) is reacted with diallyl ether (24.54g., 0.25 mole).

Sources & evidence

ORD record: ord-f4be87bce98d43eeb4fcd3187316671d
Source dataset: uspto-grants-1994_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05284886

Reaction notes

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