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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582308Generated: October 25, 2026

Diisobutylaluminum hydride → 4-(Oxazol-2-yl)-benzyl alcohol

https://huagongshe.com/reaction/1582308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantMethyl 4-(oxazol-2-yl)benzoateHCID 21985208—
SolventDichloromethaneHCID 6344—
Product4-(Oxazol-2-yl)-benzyl alcoholHCID 2072562489%

Reaction Steps

To a solution of methyl-4-(oxazol-2-yl)-benzoate (0.203 g, 1 mmol) in CH2Cl2 (10 mL) 0° C. was added DIBAL-H (4 mL of a 1.0M solution in dichloromethane, 4 mmol) over 10 min. The resultant solution was stirred at 0° C. for 2 h then quenched with an aqueous saturated solution of sodium potassium tartrate (20 mL) and the biphasic mixture stirred rapidly for 60 min. The phases were separated and the aqueous layer extracted with CH2Cl2 (3×10 mL). The combined organic fractions were dried (Na2SO4), filtered, concentrated and purified by chromatography on silica gel (10:1 CH2Cl2/MeOH) to afford the title alcohol (0.156 g, 89%). 1H NMR (CDCl3) δ3.42 (t, 1H, J=6.0 Hz (OH)), 4.77 (s, 2H, J=6.0 Hz), 7.24 (s, 1H), 7.47 (d, 2H, J=7.8 Hz), 7.71 (s, 11H), 8.05 (d, 2H, J=7.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734191B2
Source datasetuspto-grants-2004_05
ORD IDord-2bf8a15c017c4e3698feae1307b7c0d7
Source noteuspto-grants-2004_05