HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82952Generated: October 25, 2026
Sodium hydride → Tert-butyl 3-(1,3-thiazol-2-ylmethoxy)azetidine-1-carboxylate
https://huagongshe.com/reaction/82952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tert-butyl 3-hydroxyazetidine-1-carboxylate | HCID 2756801 | — |
| Reactant | 2-(Chloromethyl)-1,3-thiazol-3-ium chloride | HCID 67154570 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | Tert-butyl 3-(1,3-thiazol-2-ylmethoxy)azetidine-1-carboxylate | HCID 67154588 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846711B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-7a0d70ddefcc4ea195d5546260264ea3 |
|---|
| Source note | uspto-grants-2014_09 |
|---|