HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414176Generated: October 26, 2026
Bis(3-hydroxyphenyl)ethane-1,2-dione → 1,2-Bis(3-hydroxyphenyl)ethanone
https://huagongshe.com/reaction/1414176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(3-hydroxyphenyl)ethane-1,2-dione | HCID 13158606 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,2-Bis(3-hydroxyphenyl)ethanone | HCID 14774134 | 31.1% |
Reaction Steps
A mixture of 3,3'-dihydroxybenzil (3.0 g.) and powdered zinc (5.0 g.) in N,N-dimethylformamide (25 ml.) and water (10 ml.) was stirred and heated under reflux for 6 hours. The cooled mixture was filtered through Celite and the filtrate was evaporated under oil pump vacuum to give a syrup. The syrup was dissolved in ethyl acetate and the solution was washed consecutively with dilute hydrochloric acid and saturated brine (thrice). The dried (MgSO4) solution was evaporated to smaller volume and benzene was added. A by-product (0.45 g., m.p. 225°-228°) crystallized on standing. The mother liquor was evaporated to a syrup which was crystallized by seeding from ethyl acetate benzene to give the title product (0.88 g., m.p. 151°-154°) which was shown to be identical with material produced from the two stage reduction (1, Sn/HCl; 2, Zn/chromic sulfate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001216 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-207cc7d6a0bd4781a2dee3735e32833d |
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| Source note | uspto-grants-1977_01 |
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