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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523642Generated: October 30, 2026

Sodium Thiosulfate → Methyl 3-(4-benzyloxyazepan-1-yl)sulfonyl-4-(2-hydroxyethyl)benzoate

https://huagongshe.com/reaction/523642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 4-allyl-3-(4-benzyloxyazepan-1-yl)sulfonyl-benzoateHCID 118222059—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(4-benzyloxyazepan-1-yl)sulfonyl-4-(2-hydroxyethyl)benzoateHCID 11822204353.88%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of methyl 4-allyl-3-(4-benzyloxyazepan-1-yl)sulfonyl-benzoate (630.00 mg, 1.42 mmol, 1.00 Eq) in THF (10 mL) and H2O (2 mL) were added OsO4 (36.10 mg, 142.00 umol, 0.10 Eq) and NaIO4 (607.45 mg, 2.84 mmol, 2.00 Eq) at 0° C. The mixture was stirred at 25° C. for 3 hr. TLC detected the reaction was complete, the mixture was poured into saturated Na2S2O3 solution, extracted with DCM, the combined organic layer was dried over anhydrous Na2SO4, concentrated, the residue was diluted in MeOH (10 mL), to the formed mixture was added NaBH3CN (88.86 mg, 1.41 mmol, 1.00 Eq). The mixture was stirred at 25° C. for 3 hr. TLC detected the reaction was complete, the reaction was quenched with water, extracted with EA, the combined organic layer was dried over anhydrous Na2SO4, concentrated, the residue was purified by chromatography (silica gel, eluting with PE:EA=3:1 to 1:1) to afford product methyl 3-(4-benzyloxyazepan-1-yl)sulfonyl-4-(2-hydroxyethyl)benzoate (340.00 mg, 759.71 umol, 53.88% yield). LCMS: 448 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09339510B2
Source datasetuspto-grants-2016_05
ORD IDord-554d46fa19c6402da6f9e0a0027e5a44
Source noteuspto-grants-2016_05