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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808235Generated: October 26, 2026

Hydrogen Peroxide → Tert-butyl 6-(hydroxymethyl)-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1808235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
Reactanttert-Butyl 6-methylidene-1,4-oxazepane-4-carboxylateHCID 21064050—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductTert-butyl 6-(hydroxymethyl)-1,4-oxazepane-4-carboxylateHCID 57732267—

Reaction Conditions

Temperature25 °C

Reaction Steps

1M borane in THF (450 mL, 0.45 mol, 0.9 eq) was added under stirring and cooling on an ice bath to a stirred in a stream of argon solution of tert-butyl 6-methylene-1,4-oxazepane-4-carboxylate (Preparation 79, 107 g, 0.5 mol, 1 eq) in THF (300 mL). The reaction mixture was heated to 25° C. and stirred at this temperature for 3 h. Then the reaction mixture was cooled to 0-10° C. and treated at this temperature sequentially with 3N sodium hydroxide (170 mL) and 30% hydrogen peroxide (66 mL). The obtained homogenous mixture was stirred overnight, then treated with hexane (45 mL), and dried over potassium carbonate. The organic layer was decanted from the precipitate, which was washed with DCM. The organic layers were evaporated in vacuo, and the residue was purified rapidly (due to instability of the product on silica gel) by chromatography (carbon tetrachloride/chloroform/isopropanol 100:0:0→0:100:0→0:90:10) on silica gel (1.2 kg; 63-100 μm) to give title compound as a colorless oil in (85 g, 0.368 mol, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-294a4c1b9609470eb4d122bdbf94bd09
Source noteuspto-grants-2013_01