HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703786Generated: October 27, 2026
Acetaldehyde → 1-(4'-Trifluoromethyl-biphenyl-4-yl)-ethanol
https://huagongshe.com/reaction/1703786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 4-Bromo-4'-(trifluoromethyl)biphenyl | HCID 12712349 | — |
| Catalyst | Bromine | HCID 24408 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4'-Trifluoromethyl-biphenyl-4-yl)-ethanol | HCID 22760332 | — |
Reaction Steps
To a stirred suspension of 1.5 g of magnesium turnings in 10 ml of dry tetrahydrofuran, add a small amount of 4'-trifluoromethyl-4-bromo[1,1']biphenyl and a few drops of bromine. When the reaction is started, add (dropwise) a solution of 16 g of 4'-trifluoromethyl-4-bromo-[1,1']biphenyl in 50 ml of tetrahydrofuran at 50°-60° C. Heat the mixture for one hour, cool to 0° C., and slowly (dropwise) add 7 g of acetaldehyde. Stir the reaction mixture at room temperature for twenty hours. Work-up the reaction mixture following the procedure of example 2, and isolate the desired product by chromatography, m.p. 116°-117°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04125612 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-fa52e0b551834cedb292336b24ee4b2d |
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| Source note | uspto-grants-1978_11 |
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