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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172008Generated: October 29, 2026

Sodium hydride → Tert-butyl 3-(1,3-thiazol-2-ylmethoxy)azetidine-1-carboxylate

https://huagongshe.com/reaction/2172008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 3-hydroxyazetidine-1-carboxylateHCID 2756801—
Reactant2-(Chloromethyl)-1,3-thiazol-3-ium chlorideHCID 67154570—
CatalystWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
ProductTert-butyl 3-(1,3-thiazol-2-ylmethoxy)azetidine-1-carboxylateHCID 6715458848%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-Boc-azetidin-3-ol (260 mg, 1.5 mmol) in DMF (3.5 mL) at 0° C. under nitrogen was added NaH (60% in oil, 126 mg, 3.15 mmol). The suspension was stirred for 0.5 h at 0° C. then treated with 2-(chloromethyl)-1,3-thiazol-3-ium chloride (510 mg, 3.0 mmol; which may be prepared as described in Step 1) dissolved in DMF (1 mL) and DIPEA (1.05 mL). The mixture was allowed to warm to room temperature then heated to 80° C. overnight. The reaction mixture was cooled, water (20 drops) was added and the mixture concentrated under reduced pressure. The crude material was purified on column chromatography (eluent: Pentane/EtOAc, 90/10 to 50/50) to give the product (193 mg, 48%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051321B2
Source datasetuspto-grants-2015_06
ORD IDord-778c66f41c274567b59cd3d059c4b9b2
Source noteuspto-grants-2015_06