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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713150Generated: October 25, 2026

Tetrahydrofuran → Tert-butyl 2-methyl-6-oxo-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/713150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTert-butyl 2-methyl-6-methylene-1,4-oxazepane-4-carboxylateHCID 77508926—
ProductTert-butyl 2-methyl-6-oxo-1,4-oxazepane-4-carboxylateHCID 7750892378.48%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a mixture of tert-butyl 2-methyl-6-methylene-1,4-oxazepane-4-carboxylate (2.40 g, 10.56 mmol, 1.00 eq) in THF (50.00 mL), was added NaIO4 (4.97 g, 23.23 mmol, 2.20 eq) and K2OSO4 (401.83 mg, 2.11 mmol, 0.20 eq) in one portion at 30° C. under N2. The mixture was stirred at 30° C. for 5 hours. TLC showed the reaction was completed. The mixture was poured into saturated NaSO3 (100 mL) and stirred for 5 min. The aqueous phase was extracted with ethyl acetate (30 mL*2). The combined organic phase was washed with saturated brine (30 mL*2), dried with anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography (Petroleum ether/Ethyl acetate=8/1) to afford tert-butyl 2-methyl-6-oxo-1,4-oxazepane-4-carboxylate (1.90 g, 8.29 mmol, 78.48% yield) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181288B2
Source datasetuspto-grants-2015_11
ORD IDord-3b83e078ab2941bd9d3697519bb5b6c3
Source noteuspto-grants-2015_11