HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289228Generated: October 30, 2026
Hydrochloric Acid → 2-[(1,1'-Biphenyl)-3-yl]ethanol
https://huagongshe.com/reaction/2289228
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | 3-Bromobiphenyl | HCID 16449 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[(1,1'-Biphenyl)-3-yl]ethanol | HCID 10703117 | — |
Reaction Steps
To a solution of 3-bromobiphenyl (18 g, 77 mmol) in diethyl ether (150 ml) under N2 cooled to -78° C. was added 1.6 M t-butyl lithium in pentane (100 ml, 0.16 mole) vi a cannula over a 15 minute period. The solution was stirred 30 minutes at -78° C., ethylene oxide (9 g, 0.2 mole added and the reaction mixture allowed to warm to room temperature over a 1 hour period. The solution was boiled briefly to drive off excess ethylene oxide, transferred to a separatory funnel, a small volume of water added, and neutralized with concentrated HCl. The organic solution was dried (MgSO4) concentrated in vacuo a nd the residue purified by chromatography on silica gel eluting with ethyl acetate:hexane (1:4) to give 2-(3-biphenylyl)ethanol (10.5 g). 1H NMR (CDCl3, 60 MHz) δ: 2.81 (t, J=7 Hz, 2H, CH2), 3.76 (t, J=7 Hz, 2H, CH2) , 6.95-7.70 (m, 9H, Ar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06090941 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-69d54080ea9a4b78a51e255c0aaeed0d |
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| Source note | uspto-grants-2000_07 |
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