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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tert-butyl 2-methyl-6-methylene-1,4-oxazepane-4-carboxylate | HCID 77508926 | — |
| Product | Tert-butyl 2-methyl-6-oxo-1,4-oxazepane-4-carboxylate | HCID 77508923 | 78.48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181288B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-3b83e078ab2941bd9d3697519bb5b6c3 |
|---|
| Source note | uspto-grants-2015_11 |
|---|