HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → 17beta-Hydroxymethyl-3beta-hydroxy-6-t-butylcarboxy-6-azaandrost-4-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 17beta-Carbomethoxy-6-t-butylcarboxy-6-azaandrost-4-en-3-one | HCID 86749035 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 17beta-Hydroxymethyl-3beta-hydroxy-6-t-butylcarboxy-6-azaandrost-4-ene | HCID 86749706 | — |
Reaction Steps
A solution of 17β-carbomethoxy-6-t-butylcarboxy-6-azaandrost-4-en-3-one (2.30 g, 5.33 mmol), Example 3, part E, in methylene chloride (70 mL) at -78° C. is treated with diisobutylaluminum hydride (1.5M in toluene, 15 mL, 22.5 mmol). After 20 minutes the reaction is quenched with methanol (4 mL), methylene chloride added (150 mL), washed with 2N NaOH and water, dried over MgSO4 and concentrated to give crude 17β-hydroxymethyl-3β-hydroxy-6-t-butylcarboxy-6-azaandrost-4-ene of sufficient purity to carry on to the following steps; yield: 2.16 g (99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05543406 |
| Source dataset | uspto-grants-1996_08 |
| ORD ID | ord-49054d83773444c0aac174ca65c38a53 |
| Source note | uspto-grants-1996_08 |