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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235321Generated: October 28, 2026

Diisobutylaluminumhydride → HCID 73076084, compound

https://huagongshe.com/reaction/235321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 23367336HCID 23367336—
SolventTolueneHCID 1140—
ProductHCID 73076084HCID 7307608459.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diisobutyl aluminum hydride (6 mL, 9 mmol, 1.5M in toluene) was added to a solution of the ester 14 (0.56 g, 1.3 mmol) in anhydrous toluene (20 mL) at -78° C. After 20 min the solution was warmed to 0° C. and stirred for 1 h. The solution was slowly quenched by adding to a stirred 0° C. solution of 2N potassium sodium tartrate. Ethyl acetate was added and the organic layer separated and the water phase extracted with ethyl acetate. The combined organic phase was washed with brine, dried over anhydrous MgSO4, filtered and evaporated. The material was further purified by column chromatography on silica gel with ethyl acetate hexane mixtures to give the diol 15 (0.3 g, 59%) 1H NMR (CDCl3, 500 MHz) δ0.11 (s, 3H), 0.12 (s, 3H), 0.14 (s, 3H), 0.16 (s, 3H), 0.90 (s, 9H), 0.91 (s, 9H), 1.28 (dd, 1H), 1.43 (dd, 1H), 2.00 (ddd, 3H), 2.16 (dd, 1H), 3.33 (dd, 1H), 3.40 (dd, 1H), 4.34 (m, 2×1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597932
Source datasetuspto-grants-1997_01
ORD IDord-7c1aff2fdaaa400393eeaa3ecacc1e9a
Source noteuspto-grants-1997_01