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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium | HCID 223 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | (3R,7R)-1-bromo-3,7,11-trimethyldodecane | HCID 13191851 | — |
| Reactant | (S)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-1,2-epoxy-butane | HCID 18602184 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04824972 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-45ee9a40b9c84dffb8d5f6c96f22eb63 |
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| Source note | uspto-grants-1989_04 |
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