HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 25171020, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (R,R)-Chiraphos | HCID 2724948 | — |
| Reactant | HCID 87079984 | HCID 87079984 | — |
| Catalyst | 19584-30-6 | HCID 9940312 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 25171020 | HCID 25171020 | — |
Reaction Steps
A solution of 2-(3-(methoxypropoxy)-4-methoxybenzylidene) -3-methylbutanal (7.0 mmol, 74% E and 26% Z), tetrarhodium dodecacabonyl (0.14 mmol), (2R,3R)-(+)-2,3-Bis-(Diphenylphosphino)butane (R, R-Chiraphos, 0.63 mmol) and 300 ul triethylamine in toluene (75 ml) was transferred into an autoclave. The mixture was hydrogenated at 70-80° C. and 20 bar H2. After 42 hr additional tetrarhodium dodecacarbonyl (0.14 mmol) was added to complete the reaction in 62 hr. The mixture was concentrated to 3.5 g black oil and purified by flash chromatography (heptane/ethyl acetate=2/1). Yield=1.6 g yellow oil (74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088955B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-8518ceaeebf644c89ccad75cf15a3f7f |
| Source note | uspto-grants-2012_01 |