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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734666Generated: November 1, 2026

2-Chlorobenzoxazole → 4-(Benzoxazol-2-yl)benzyl alcohol

https://huagongshe.com/reaction/1734666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(Benzoxazol-2-yl)benzyl alcoholHCID 15389017—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To 500 ml THF cooled to -78° C. is added butyl lithium (2 eq.) followed by 4-bromobenzyl alcohol (27.2 g; 145 mmol) slowly over 45 minutes in a solution of THF (100 ml) keeping the temperature below -72° C. After 10 minutes following the final addition of the alcohol is added 2-chlorobenzoxazole (23.3 g; 145 mmol) in 25 ml THF slowly over 45 minutes. The temperature is maintained at -78° C. for 1 hour and then warmed to -40° C. for 15 minutes. The reaction is then quenched with 15 ml of acetic acid and allowed to warm to room temperature, diluted with 800 ml ether, washed 3x with H2O and brine, dried (MgSO4) and concentrated in vacuo to obtain a brown oily solid which is washed with 400 ml petroleum ether and filtered to obtain 4-(benzoxazol-2-yl)benzyl alcohol as a tan solid which is used directly in Step B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534532
Source datasetuspto-grants-1996_07
ORD IDord-d7d5b124225c43ae933c80490a3c2f3a
Source noteuspto-grants-1996_07