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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893609Generated: October 30, 2026

Trifluoroacetic acid → HCID 14606665, compound

https://huagongshe.com/reaction/893609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86745953HCID 86745953—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14606665HCID 14606665—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (3S-trans)-tetrahydro-5-(dimethoxymethyl)-3-furanol-4-methylbenzenesulfonate, (Compound IV(e), 10.0 g, 31.6 mmole), 1% CF3CO2H (50 mL), and dioxane (80 mL) in a 250 mL round bottom flask fitted with a reflux condenser was warmed to 80° C. for five hours. After cooling to room temperature, the solution was adjusted to pH 7.0 using 1N NaOH, treated with NaBH4 (1.2 g, 31.7 mmole), and allowed to stir at room temperature for an additional 30 minutes. The solvent was partially removed, then extracted with EtOAc (100 mL×3). The organic fraction was dried over MgSO4, filtered, evaporated and purified by flash column chromatorgraphy (60% EtOAc/40% Hexane) to afford 3.6 g or recovered starting material and 2.7 g (49% based on recovered starting material) of Compound IV(c).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126347
Source datasetuspto-grants-1992_06
ORD IDord-32006c7b986c4262be99a978949e5dec
Source noteuspto-grants-1992_06