HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isobutyraldehyde → HCID 11041200, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isobutyraldehyde | HCID 6561 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | D-HOMOCYSTEINE THIOLACTONE HYDROCHLORIDE | HCID 10130065 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11041200 | HCID 11041200 | — |
Reaction Steps
4.6 mmol of triethylamine are added at 0° C., under an inert atmosphere, to a solution of 4.23 mmol of D-homocysteine thiolactone hydrochloride and 8.46 mmol of isobutyraldehyde in 20 ml of methanol. After stirring for 4 hours at ambient temperature, the reaction mixture is cooled to 0° C. and 8.8 mmol of NaCNBH3 are slowly added in the course of 40 minutes. After stirring for 30 minutes at 0° C., the reaction mixture is hydrolysed and then extracted with ether. The combined organic phases are then washed with a saturated NaCl solution, dried over sodium sulphate, filtered and concentrated under reduced pressure. Chromatography on silica gel (dichloromethane/methanol: 99/1) allows the expected product to be isolated in the form of syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063816 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-577e08151b95438da8c842d4732e229f |
| Source note | uspto-grants-2000_05 |