Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358937Generated: October 30, 2026

Citric Acid → HCID 14793480, compound

https://huagongshe.com/reaction/358937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantLithium ChlorideHCID 433294—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15099993HCID 15099993—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14793480HCID 1479348078.7%

Reaction Steps

A solution of 2.28 g(13.5 mM) of (-)-ethyl 2-cyano-2-methylpentanoate in 22 ml of dry tetrahydrofuran was added dropwise to a mixture of 1.14 mg (27.0 mM) of anhydrous lithium chloride and 1.02 mg (27.0 mM) of sodium borohydride under stirring at room temperature. Then, 44 ml of dry ethanol was added thereto, followed by 16 hours of reaction at room temperature. After the reaction, while the reaction mixture was cooled on an ice bath, 10% citric acid was added until the pH reached 4. A white solid recipitated at this time was separated by filtration, and the solvent was removed from the filtrate by reduced pressure distillation. Then, 5 ml of distilled water was added to the product, followed by extraction with dichloromethane. The resultant organic layer was dried on sodium sulfate, followed by distilling-off of the solvent under reduced pressure and further distillation to obtain 9.35 mg(10.6 mM) of (+)-2-cyano-2-methylpentanol. Yield:78.7%, b.p. 110° C.; [α]D -0.9 degree, [α]435 -1.6 degree (c1, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04999130
Source datasetuspto-grants-1991_03
ORD IDord-f88bda3174744e6f87f63a967acff330
Source noteuspto-grants-1991_03