HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 3beta-tert-Butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5alpha-chola-8,14-dien
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3beta-Tert-butyidimethylsilyloxy-4,4-dimethyl-5alpha-chola-8,14-dien-24 oic acid | HCID 69410795 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3beta-tert-Butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5alpha-chola-8,14-dien | HCID 69411663 | — |
Reaction Steps
3β-tert-Butyldimethylsilyloxy-4,4-dimethyl-5α-chola-8,14-dien-24 oic acid (0.15 g) is reacted with aniline following the procedure outlined in example 10 and reduced with lithium aluminum hydride (0.15 g) in THF at room temperature. Aqueous work-up and. crystallization from methanol gives 3β-tert-butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5α-chola-8,14-dien (106 mg). 1H-NMR (CDCl3, 300 MHz)): δ=7.17 (2H, t); 6.69 (1H, t); 6.6 (2H, d); 5.35 (1H, s); 3.6 (1H, s); 3.2 (1H, m); 3.09 (2H, m); 0.9 (9H, s); 0.04 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06407086B2 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-5ebb9ac32f994232b4f8e0d9755ba8fe |
| Source note | uspto-grants-2002_06 |