HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569309Generated: October 30, 2026
2-Hydroxyisobutyric acid → HCID 53668099, compound
https://huagongshe.com/reaction/569309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxyisobutyric acid | HCID 11671 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 20148928 | HCID 20148928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53668099 | HCID 53668099 | — |
Reaction Steps
{[9a-(Acetoxyethyl)-5,6-dichloro-3-oxo-2,3,9,9a-tetrahydro-1H-fluoren-7-yl]oxy}acetic acid (4.13 g, 10 mMole) is dissolved in dry tetrahydrofuran (20 ml). 1,1'-Carbonyldiimidazole (3.2 g, 10 mMole) is added and the mixture stirred at 20° C. for an hour. 2-Hydroxy-2-methylpropionic acid (1.05 g, 10 mMole) is added and the mixture stirred for 18 hours at 20° C. The solvent is removed by evaporation in vacuo. The residue is dissolved in methylene chloride, washed with water and dried over MgSO4. The solvent is removed by evaporation in vacuo and the residue purified by chromatography using a silica gel column with methylene chloride/tetrahydrofuran/acetic acid 100/2/1 (V.V.V.) as the eluent. Selecting the appropriate cuts gave the desired compound upon evaporation of the solvent in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04731471 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-127353321aa74dda8d5621238af7e372 |
|---|
| Source note | uspto-grants-1988_03 |
|---|