HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484051Generated: October 31, 2026
Hydroxyphenylacetic acid → HCID 19748801, compound
https://huagongshe.com/reaction/484051
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyphenylacetic acid | HCID 127 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19748801 | HCID 19748801 | 93.9% |
Reaction Steps
To a solution of 4-hydroxyphenylacetic acid (50.0 gm, 0.33 mol) in DMSO (300 mL) was added 50% aqueous NaOH (57.0 gm, 0.71 mol) with stirring. After stirring for 10 min at room temperature bromoacetaldehyde diethyl acetal (66.0 gm, 0.33 mol) was added. The solution was heated at 100°-110° C. for 2 hr when an additional 2 gm of 50% NaOH was added. After heating for another hour the reaction mixture was cooled and poured into a mixture of aqueous HCl (30 mL of conc. HCl in 400 mL ice-H2O) and Et2O. The layers were separated and hexane was added to the Et2O layer. The organic layer was washed successively with H2O (twice) and saturated NaCl before being dried over Na2SO4, filtered and evaporated to dryness to give 83.7 gm (0.31 mol) of 4-[(2,2-diethoxy)ethoxy]phenylacetic acid which was suitable for use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05229381 |
|---|
| Source dataset | uspto-grants-1993_07 |
|---|
| ORD ID | ord-80284cc62f9d4c149aee653b752e78d8 |
|---|
| Source note | uspto-grants-1993_07 |
|---|