Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 54342988 | HCID 54342988 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54278690 | HCID 54278690 | — |
Reaction Steps
iv)—A solution of the aldehyde (12.3 g) mentioned above in dry pyridine (150 ml) was cooled to 4° C. Benzoyl chloride (8 ml) was added in 5 min. and the reaction mixture was stirred for 1.5 h at room temperature. Then it was poured into water (2 l) and the resulting mixture was stirred overnight. The product was extracted into dichloromethane and the combined organic phases were concentrated under reduced pressure to give (3β,5α,20R)-3-(benzoyloxy)-4,4,20-trimethylpregna-8,14-diene-21-carboxaldehyde (16.1 g). The product was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06177420B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-253a17a007a54d07b327bbadce7e74ee |
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| Source note | uspto-grants-2001_01 |
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