Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 54301022 | HCID 54301022 | — |
| Product | HCID 67791828 | HCID 67791828 | — |
Reaction Steps
1.2 g (3.23 mmol) of 2-hydroxy-4-[2-hydroxy-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2naphthyl)ethoxy]benzyl alcohol and 30 ml of pyridine are introduced into a flask and 345 ml (4.84 mmol) of acetyl chloride are added. The reaction mixture is stirred at 0° C. for 4 hours. It is poured into water, acidified with hydrochloric acid and extracted with ethyl acetate. The extract is washed with water, and the organic phase is separated, dried over sodium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column, eluted with a mixture of hexane and ethyl acetate (70:30). After evaporation of the solvents, 140 mg (10.4%) of the expected product are collected in the form of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05476860 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-5c52acadcf2847e3a2d44f189d4e5af9 |
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| Source note | uspto-grants-1995_12 |
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