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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035403Generated: October 30, 2026

Water → Tert-butyl 1-oxa-6-azaspiro[2.6]nonane-6-carboxylate

https://huagongshe.com/reaction/2035403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantN-Boc-hexahydro-1H-azepin-4-oneHCID 1512679—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 1-oxa-6-azaspiro[2.6]nonane-6-carboxylateHCID 57366410240.8%

Reaction Steps

to a stirred solution of trimethylsulfoxonium iodide (56.1 g, 255 mmol) in anhydrous DMSO (150 ml) was added a mixture of NaH (18.5 gram 1.5 equiv., 60% in mineral oil) under a nitrogen atmosphere. The mixture was stirred at 65° C. for 1 hour, whereafter compound 2 (32 g, 150 mmol) was added as a solution in DMSO (10 ml). The mixture was refluxed overnight under a nitrogen atmosphere. The solution was allowed to reach room temperature, water was added and the mixture was extracted with diethyl ether (3×200 ml). The combined organic layer was washed with H2O, with brine and dried over Na2SO4. The Et2O was evaporated to yield 82.1 gram (32 g, 95%) compound 3. 1H-NMR (300 MHz, CDCl3): δ (ppm)=1.45 (s, 9H, BOC); 1.50-2.10 (m, 6H), 2.60-2.70 (m, 2H), 3.5-3.60 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575148B2
Source datasetuspto-grants-2013_11
ORD IDord-8019f0b1de244834855a5055a6c95c5b
Source noteuspto-grants-2013_11