HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diketene → 1-Benzylpiperidin-3-yl 3-oxobutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diketene | HCID 12661 | — |
| Reactant | 1-Benzylpiperidin-3-ol | HCID 85773 | — |
| Product | 1-Benzylpiperidin-3-yl 3-oxobutanoate | HCID 13519357 | 62.7% |
Reaction Steps
Then, 11.8 g of the 1-benzyl-3-hydroxypiperidine and 5.6 g of diketene were reacted similarly as in Reference Example 1, and the reaction product was purified by silica gel column chromatography (eluent:chloroform:methanol=9:1 v/v), to obtain 10.65 g of acetoacetic acid-N-benzyl-3-piperidinyl ester (yield: 62.5%). This was used in the reaction of Example 4 without distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04448964 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-6995a1bc01b3463fa28fbe308a99dda6 |
| Source note | uspto-grants-1984_05 |