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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798794Generated: November 2, 2026

Methanol → HCID 58128481, compound

https://huagongshe.com/reaction/1798794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantHCID 10516122HCID 10516122—
SolventDichloromethaneHCID 6344—
ProductHCID 58128481HCID 58128481—

Reaction Conditions

Temperature0 °C

Reaction Steps

1 M DiBAl—H in dichloromethane (42 mL, 2.2 eq.) was added slowly, via an addition funnel, over 20 min to a well stirred solution of the α,β-unsaturated ester from step 1 of this example (5.14 gram, 1 eq.) in anhydrous DCM (100 mL) under argon atmosphere at −78° C. The resulting solution was warmed to 0° C. after completion of addition and was kept at that temperature for 30 min. The reaction was cooled back to −78° C. and 4 mL MeOH was added slowly to quench the excess DiBAl-H. The cold solution was further stirred at −78° C. for 10 min before pouring into 150 mL saturated aqueous Rochelle (sodium potassium tartrate) salts solution. The mixture was vigorously stirred at room temperature for 3 hours until it turned clear. The organic layer was separated, dried over sodium sulfate, filtered and concentrated i. vac. The residue was further purified by column chromatography using acetone/hexanes (20%, isocratic) to give the desired product as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343990B2
Source datasetuspto-grants-2013_01
ORD IDord-c5f19fb3e2ba442cbf3209efea711df6
Source noteuspto-grants-2013_01