HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86743005, compound → HCID 86743007, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86743005 | HCID 86743005 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86743007 | HCID 86743007 | — |
Reaction Steps
10.58 g of (6E)-10-(tert.-butyldimethylsiloxy)-3,7,11-trimethyl-2,6,11-dodecatrien-1-ol are added dropwise at 0° to a suspension of 110 g of manganese dioxide (precipitated, active) in 220 ml of dichloromethane and the mixture is stirred at room temperature for 2 hours. After filtration over Hyflo the filtrate is concentrated and oily residue is chromatographed on silica gel with hexane-ethyl acetate-triethylamine 90:10:0.1. There is obtained (6E)-10-(tert.-butyldimethylsiloxy)-3,7,11-trimethyl-2,6,11-dodecatrienal as a yellowish oil. NMR (80 MHz, CDCl3): 10.1 (d, J=8, H-C(1)); 6.0 (d, J=8, H-C(2)); 5.2 (m, H-C(6)); 5.0-4.8 (m, 2H-C(12)); 4.1 (t, J=6.5, H-C(10)); 2.4-1.4 (m, 4CH2, 3CH3); 0.95 (s, SiC(CH3)3); 0.1 and 0.05 (2s, Si(CH3)2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04827004 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-b796d8e5831042a6a5d05632706dbe20 |
| Source note | uspto-grants-1989_05 |