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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093988Generated: October 27, 2026

Diisobutylaluminum hydride → 5-(Hydroxymethyl)-1,3-Dihydro-2H-Indol-2-One

https://huagongshe.com/reaction/1093988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantSodium HydroxideHCID 14798—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantEthyl 2-oxoindoline-5-carboxylateHCID 13077452—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-(Hydroxymethyl)-1,3-Dihydro-2H-Indol-2-OneHCID 59751036—

Reaction Steps

To a solution/suspension of the compound obtained in Step B (66.8 mmol) in THF (850 ml) at −65° C. there is added, dropwise, 1M DIBAL-H solution (546 mmol) over one hour and under an inert atmosphere. The reaction mixture is brought to −30° C. over 1 hour 30 minutes. 22 ml of water are added dropwise and then 22 ml of 15% aqueous sodium hydroxide solution at 0° C. and then 55 ml of water. MgSO4 (300 g) is added to the reaction mixture and stirring is carried out for 30 minutes. The suspension is filtered over Celite and washed with THF. The filtrate is evaporated to dryness to yield a pasty solid that is brown in colour. The residue is triturated in methanol, and the powder obtained is filtered off and dried in vacuo to yield the title product, which is used directly in the next Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133889B2
Source datasetuspto-grants-2012_03
ORD IDord-3bd5a78a23e647d793d64ed4596fe7d8
Source noteuspto-grants-2012_03