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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621751Generated: November 2, 2026

Ammonium → 3-Hexadecanol, 3,7,11,15-tetramethyl-

https://huagongshe.com/reaction/621751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniumHCID 223—
ReactantEthyl AcetateHCID 8857—
ReactantMagnesiumHCID 5462224—
Reactant(3R,7R)-1-bromo-3,7,11-trimethyldodecaneHCID 13191851—
Reactant(S)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-1,2-epoxy-butaneHCID 18602184—
SolventDiethyl EtherHCID 3283—
Product3-Hexadecanol, 3,7,11,15-tetramethyl-HCID 3020977—

Reaction Steps

5.8 mmol of (3R,7R)-3,7,11-trimethyldodecyl bromide are heated at reflux for 1/4 hour in 20 ml of ethyl acetate with activated magnesium. Then, there are added at 0° C. 1 g of (S)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-1,2-epoxybutane and 0.9 g of copper(I)-2-propylacetylide (or 1.2 g of copper(I) bromide/dimethyl sulphide complex). The temperature of the reaction mixture is subsequently left to rise to room temperature and the mixture is stirred overnight. 10 ml of ammonium with ethyl ether. The extract is dried and concentrated, and the residue is distilled in a bulb-tube (b.p.0.01 =140° C.). There are obtained 1.28 g (72%) (or 1.41 g (79%) of (3R,7R,11R)-1-)2',5'-dimethoxy-3',4',6'-trimethylphenyl)-3,7,11,15-tetramethylhexadecan-3-ol as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824972
Source datasetuspto-grants-1989_04
ORD IDord-45ee9a40b9c84dffb8d5f6c96f22eb63
Source noteuspto-grants-1989_04