HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893609Generated: October 30, 2026
Trifluoroacetic acid → HCID 14606665, compound
https://huagongshe.com/reaction/893609
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86745953 | HCID 86745953 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 14606665 | HCID 14606665 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05126347 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-32006c7b986c4262be99a978949e5dec |
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| Source note | uspto-grants-1992_06 |
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