HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → 4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | 2-Iodo-2-methylpropane | HCID 11206 | — |
| Reactant | 1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine | HCID 688178 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 4-Benzoyloxy-1-t-butoxy-2,2,6,6-tetramethylpiperidine | HCID 12996907 | 44.5% |
Reaction Steps
A solution of 56.0 g (203 mmol) of 4-benzoyloxy-1-oxyl-2,2,6,6-tetramethylpiperidine, 125 ml of chlorobenzene, and 58.9 g of t-butyl iodide is cooled to 5° C. Tri-n-butyltin hydride (29 g, 100 mmol) is added dropwise over 110 minutes while the temperature is maintained below 20° C. The reaction mixture is concentrated at reduced pressure and then purified by silica gel chromatography (200:1, then 100:3 heptane:ethyl acetate) to afford 30.1 g of a white solid, m.p. 80°-82.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05204473 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-03b8a0f652b34942ad38273eb81f18a7 |
| Source note | uspto-grants-1993_04 |