HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089348Generated: October 30, 2026
Isobutylene → isopropyl (R)-2-hydroxy-4-methyl-4-pentenoate
https://huagongshe.com/reaction/1089348
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Isopropyl glyoxylate | HCID 10920483 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | isopropyl (R)-2-hydroxy-4-methyl-4-pentenoate | HCID 53635694 | 78% |
Reaction Steps
A solution of an (R)-binaphthol-dichlorotitanium complex which had been prepared in the same manner as in Example 1 was cooled to -70° C., into which was bubbled 0.56 g (10 mmoles) of 2-methyl-l-propene, followed by adding thereto 116 mg (1 mmole) of isopropyl glyoxylate. Subsequently, the mixture was reacted at -30° C. for 15 hours. Then, 10 ml of an aqueous sodium hydrogen carbonate solution was added to terminate the reaction. The reaction mixture was filtered through Celite and extracted with two 20 ml portions of diethyl ether and two 20 ml portions of ethyl acetate, and the extract was dried over anhydrous magnesium sulfate. Thereafter, the solvents were distilled off, and the residue was purified by means of silica gel column chromatography to obtain 0.13 g of isopropyl (R)-2-hydroxy-4-methyl-4-pentenoate. The yield was 78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04965398 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-69bb6141c6724a00a8403444ce5a25a5 |
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| Source note | uspto-grants-1990_10 |
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