HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22501Generated: October 26, 2026
Hydrochloric Acid → 4-(2-Hydroxyethoxy)mandelic acid
https://huagongshe.com/reaction/22501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (+-)-4-Hydroxymandelic acid | HCID 328 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Hydroxyethoxy)mandelic acid | HCID 19930444 | 89.3% |
Reaction Steps
1040.8 g (5.00 mol) of 4-hydroxymandelic acid, sodium salt monohydrate, 10.0 g (0.25 mol) of sodium hydroxide and 1000 ml of water are placed in an autoclave of 6.3 liter capacity. The autoclave is flushed with nitrogen and 330.4 g (7.50 mol) of ethylene oxide are then injected. The contents are slowly heated to 95° C. over a period of 2 hours with stirring and stirred at this temperature for another 2 hours. The still hot reaction mixture is poured into another vessel, acidified at 95° C. with 540 ml (about 5.5 mol) of 32% hydrochloric acid and crystallized by slow cooling to about +10° C. The precipitated product is filtered with 1000 ml of cold water and dried to give 948 g (89%) of 4-(2-hydroxyethoxy)mandelic acid, m.p. 162°-164° C. (compound (201), Table 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05428162 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-c67edfe10f0c42c1817b3ec1f6f83abd |
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| Source note | uspto-grants-1995_06 |
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