HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205253Generated: October 25, 2026
Tin tetrachloride → HCID 121003791, compound
https://huagongshe.com/reaction/2205253
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | HCID 535486 | HCID 535486 | — |
| Reactant | Cyclohexanone, 2-(1-methylethenyl)- | HCID 11018939 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 121003791 | HCID 121003791 | 84% |
Reaction Steps
An argon flushed three-necked flask which was cooled by an ice-water bath was charged with 2-(prop-1-en-2-yl)cyclohexanone (0.88 g, 6.38 mmol), acetaldehyde O-methyl oxime (0.56 g, 7.65 mmol), and SnCl4 (1.66 g, 6.38 mmol) in 1,2-dichloroethane (65 ml). The mixture was stirred for 48 hours at room temperature. The completion of reaction was checked by GC analysis of reaction aliquots quenched with a solution of saturated NaHCO3 in water. The reaction mixture was quenched with sat. aqueous NaHCO3 solution (50 mL). The organic phase was separated and the aqueous layer was extracted with MTBE three times. The combined organic layers were washed with brine (30 mL), dried (MgSO4) and evaporated in vacuo. The crude product was purified by distillation under reduced pressure to yield the title product as a colorless liquid (1.13 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09371262B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-81d5deafb28b4ac094fb9a58779f44f1 |
|---|
| Source note | uspto-grants-2016_06 |
|---|