HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859077Generated: October 26, 2026
Acetyl chloride → 3alpha-Acetylcholanic acid
https://huagongshe.com/reaction/859077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithocholic Acid | HCID 9903 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3alpha-Acetylcholanic acid | HCID 18346002 | — |
Reaction Steps
To tetrahydrofuran was added 0.1 mole of lithocholic acid and 0.1 mole of triethylamine, and the resulting solution was maintained at a temperature below 4° C. in an ice bath. 0.12 mole of acetyl chloride was slowly added thereto, and the resulting solution was reacted for 8 hours. Thereafter, residual solvent was removed by using a vacuum distillator. A compound was extracted by using ethyl acetate, and washed with water a few times, to obtain 3α-acetylcholanic acid. To tetrahydrofuran was added 0.2 mole of 3α-acetylcholanic acid thus obtained and a slight amount of p-toluensulfonic acid. 0.21 mole of ethylvinylether was added to the resulting solution. Then, the resulting solution was reacted for 12 hours, to obtain 3α-acetylethoxyethyl lithocholate of formula 3 (yield: 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07150961B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-66f90cdfab304ccfac345517ad8a44d7 |
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| Source note | uspto-grants-2006_12 |
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