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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453636Generated: October 30, 2026

2-Methyltetrahydrofuran → HCID 66673339, compound

https://huagongshe.com/reaction/453636

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethyltetrahydrofuranHCID 7301—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66674010HCID 66674010—
ReactantHCID 86631184HCID 86631184—
SolventWaterHCID 962—
ProductHCID 66673339HCID 6667333985.7%

Reaction Steps

To a slurry of sodium (S)-4-cyclohexyl-1-hydroxy-3-methoxycarbonyl-butane-1-sulfonate (25.8 g, 81.5 mmol) and 2-methyl-tetrahydro-furan (300 mL) was added 1.0 M NaOH in water (76.1 mL) and the reaction mixture was stirred for 20 min at RT. To the reaction mixture was added (6S,7S)-7-Amino-8,8-diethyl-6-methoxy-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid amide hydrochloride (17.0 g, 54.3 mmol); the reaction mixture was stirred for 40 min at RT, sodium triacetoxyborohydride (46.1 g, 217 mmol) was added in 4 portions. The reaction mixture was stirred at RT overnight after the first two portions. Water (200 mL) and MeTHF (100 mL) were added; the phases were separated and the organic layer was washed with 1 M NaOH (2×200 mL), diluted brine (200 mL) dried with Na2SO4 and solvent was removed to yield crude title intermediate (22 g) as a glassy yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492399B2
Source datasetuspto-grants-2013_07
ORD IDord-b099f3861e2e44e686efdbf12a2f3d39
Source noteuspto-grants-2013_07