Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | HCID 59271881 | HCID 59271881 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178494954 | HCID 178494954 | — |
Reaction Steps
To a solution of tert-butyl(5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyano-4-methoxy-4-methylpentyl)methylcarbamate (4.37 kg, 10.91 mol) in MeOH (28 L) at 30° C. was added aqueous hydroxylamine (50% in water, 1.2 L, 19.63 mol). The resulting mixture was heated to 40° C. overnight, then cooled and concentrated in vacuo. The crude residue was dissolved in 1.5 L of toluene, concentrated under reduced pressure, and dried in vacuo. The crude material was used in the next step without further purification. LC-MS: 434.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513234B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-ad3502af8d76402582aca39ec4ea7376 |
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| Source note | uspto-grants-2013_08 |
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