HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369112Generated: October 30, 2026
Hydrochloric Acid → [4-(3,4-Dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid
https://huagongshe.com/reaction/2369112
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3,4-Dichlorobenzyl 2-(4-((3,4-dichlorobenzyl)oxy)phenyl)-2-hydroxyacetate | HCID 66922590 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | [4-(3,4-Dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid | HCID 66923034 | — |
Reaction Steps
2-[4-(3,4-Dichloro-benzyloxy)-phenyl]-2-hydroxy-acetic acid 3,4-dichloro-benzyl ester (9.4 g,) was dissolved in 120 mL of THF-methanol (4:1) and 2N lithium hydroxide solution (39 mL) added. The resulting reaction mixture was stirred at room temperature 16 h. The mixture was poured onto 1N HCl and EtOAc and the organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residual oil was taken up in minimal DCM and hexanes added to give a solid. The solid was filtered and washed with hexanes to afford the desired product [4-(3,4-dichloro-benzyloxy)-phenyl]-hydroxy-acetic acid in pure form (6.1 g). 1H NMR (400 MHz, DMSO d6): 7.69 (d, 1H), 7.63 (d, 1H), 7.41 (m, 1H), 7.31 (m, 2H), 6.96 (m, 2H), 5.10 (s, 2H), 4.94 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703766B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-b045e81650684864a4c2bd25ac5e7888 |
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| Source note | uspto-grants-2014_04 |
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