HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475529Generated: October 26, 2026
Acetic Acid → 5-(4-(Benzyloxy)benzyl)thiazolidine-2,4-dione
https://huagongshe.com/reaction/475529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 3096180 | HCID 3096180 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dimethylglyoxime | HCID 135459645 | — |
| Catalyst | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tetrahydrofuran N,N-dimethylformamide | HCID 21974620 | — |
| Product | 5-(4-(Benzyloxy)benzyl)thiazolidine-2,4-dione | HCID 44319268 | — |
Reaction Steps
To the suspension containing CoCl2.6H2O (4.49 mg, 0.016 mmol) and dimethylglyoxime (74.54 mg, 0.64 mmol) in 10 ml of water, 4 drops of 1.0N NaOH and NaBH4 (417.1 mg, 10.85 mmol) were subsequently added. The mixture was cooled to 0° C., and 5-(4-(benzyloxy)benzylidene)thiazolidine-2,4-dione (1 g, 3.27 mmol) in 15 ml of THF-DMF (2:1) was added thereto over 20 minutes. The mixture was stirred at room temperature for 18 hours, to which acetic acid was then added until the pH thereof reached about 6. The mixture was diluted with water and extracted with ethyl acetate and water. The organic layer was washed with water several times, dried with anhydrous magnesium sulfate, filtered and solvent-evaporated. The residual oil was chromatographed on silica gel to afford 5-(4-(benzyloxy)benzyl)thiazolidine-2,4-dione (Derivative 116 of the above formula) as white solid (0.8 g, yield: 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637558B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-5aa16f9af2634ca49c29a80a16c1b3b2 |
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| Source note | uspto-grants-2014_01 |
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