HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283863Generated: October 31, 2026
Trimethylstannane → 11-(p-Tolylsulfonyl)undecyltrimethylstannane
https://huagongshe.com/reaction/1283863
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylstannane | HCID 12623 | — |
| Reactant | 10-Undecenyl-p-tolyl sulfone | HCID 21475532 | — |
| Product | 11-(p-Tolylsulfonyl)undecyltrimethylstannane | HCID 23466634 | — |
Reaction Steps
The procedure described in Example 1 was employed except that 13.1 g (42.5 mmoles) of 10-undecenyl-p-tolyl sulfone and 14.0 g (85 mmoles) of trimethyltin hydride were the reactants. The reaction mixture was irradiated for 189 hours. The excess trimethyltin hydride was allowed to evaporate from the reaction mixture under a flow of nitrogen. The residual oil weighed 15.5 g. One-half of the crude product was chromatographed on a column containing silica gel using toluene and 2% acetone in toluene as eluents. The product, 11-(p-tolylsulfonyl)-undecyltrimethylstannane, was obtained as an oil. The presence of both the sulfonyl and trimethyltin groups was indicated by the strong infrared absorption bands at 1315 cm-1, 1300 cm-1, 1285 cm-1, 1140 cm-1 (--SO2 ) and 760 cm-1 [(CH3)3Sn--]. NMR showed the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03976672 |
|---|
| Source dataset | uspto-grants-1976_08 |
|---|
| ORD ID | ord-54c802d2ee604062837dc11c63523a24 |
|---|
| Source note | uspto-grants-1976_08 |
|---|