HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-Hydroxy-1-iodo trans-1-octene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Iodo-4-trimethylsiloxy-trans-1-octene | HCID 12851277 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-1-iodo trans-1-octene | HCID 12851278 | — |
Reaction Steps
A 23 g portion of 1-iodo-4-trimethylsiloxy-trans-1-octene is dissolved in a mixture of 200 ml of glacial acetic acid, 100 ml of tetrahydrofuran, and 50 ml of water. After solution occurs, toluene is added and the mixture is evaporated. The resulting oil is chromatographed on silica gel with hexane progressively enriched in benzene followed by acetone to give 16 g of an oil, pmr spectrum (CDCl3): 3.69 (m, CHOH) and 2.3 (s, OH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04131737 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-da257bb3e6ae4e2396418af38d0051b7 |
| Source note | uspto-grants-1978_12 |