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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835647Generated: November 1, 2026

Sodium Hydroxide → (R)-Solketal

https://huagongshe.com/reaction/1835647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant5,6-Isopropylidene-L-gulonic acid gamma-lactoneHCID 10867731—
ReactantSodium periodateHCID 23667635—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(R)-SolketalHCID 73605655.7%

Reaction Steps

To a stirring suspension of the product of Preparation 2, Step B, 5,6-O-isopropylidene-L-gulono-1,4-lactone (15.16 g, 69.5 mmol) in water (0.3 L) was added solid sodium periodate in small portions at 3° C. to 5° C. The pH of the mixture was adjusted to 5.5 with 1N aqueous sodium hydroxide. The suspension was stirred for 2 hours at ambient temperature, then saturated with sodium chloride (20.0 g) and filtered. To the filtrate, at 3° C. to 5° C., was added sodium borohydride (10.5 g, 0.278 mol) in small portions. The reaction mixture was stirred for 18 hours at ambient temperature. Acetone (100 mL) was added to destroy the excess of sodium borohydride, and the stirring was continued for 30 minutes. The acetone was removed under reduced pressure, and the aqueous residue was extracted with dichloromethane (3×300 mL) and EtOAc (3×300 mL). The combined organic layers were dried over magnesium sulfate, filtered, and evaporated to give (R)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)-methanol (5.07 g, 55.7%) as a colorless clear liquid: MS (APCI+)=132.9 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770778B2
Source datasetuspto-grants-2004_08
ORD IDord-a2acc10bc71f449fb8f23caf0cc74ef0
Source noteuspto-grants-2004_08