HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → isopropyl (2R, 3S)-2-methyl-3-hydroxybutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | HCID 57102388 | HCID 57102388 | — |
| Solvent | Water | HCID 962 | — |
| Product | isopropyl (2R, 3S)-2-methyl-3-hydroxybutanoate | HCID 57270836 | — |
Reaction Steps
To 1.0 g of (2S, 5S,6S)-2-trichloromethyl-5,6-dimethyl-1,3-dioxan-4-one produced by a procedure similar to Example 1-(7) were added 0.1 ml of concentrated sulfuric acid and 10 ml of 2-propanol, stirred at room temperature for one hour, and 20 ml of water was added to effect ether extraction. The ether phase was dried over anhydrous sodium sulfate and ether was distilled off followed by distilling the residue to obtain 0.4 g of isopropyl (2R, 3S)-2-methyl-3-hydroxybutanoate of the following formula. ##STR61## (2) Repeating the procedure of Example 5-(1) except that 2-propanol was replaced with 2-butanol, 0.5 g of 1-methylpropyl (2R, 3S)-2-methyl-3-hydroxybutanoate of the following formula was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05411877 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-e524e68b961847e189e32cc1fcedfdbf |
| Source note | uspto-grants-1995_05 |