HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655112Generated: October 25, 2026
tert-Butyldimethylsilyl chloride → 3-((tert-Butyldimethylsilanyl)oxy)azetidine
https://huagongshe.com/reaction/655112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Hydroxyazetidine hydrochloride | HCID 2759290 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-((tert-Butyldimethylsilanyl)oxy)azetidine | HCID 57438656 | 74% |
Reaction Steps
A solution of tert-butylchlorodimethylsilane (12.01 g, 79.69 mmol) in DCM (20 mL) was added dropwise to a stiffed solution of azetidin-3-ol hydrochloride (CAS no. 18621-18-6) (8.73 g, 79.69 mmol) and anhydrous N-ethyl-N-isopropylpropan-2-amine (34.1 mL, 199.22 mmol) in DCM (20 mL) cooled to 10° C., over a period of 2 minutes under nitrogen. The resulting solution was stirred at ambient temperature for 20 hours. The reaction mixture was concentrated, diluted with EtOAc (75 mL), and washed sequentially with saturated NaHCO3 (25 mL), water (20 mL), and saturated brine (20 mL). The organic layer was dried (MgSO4), filtered and evaporated to afford the product (11.1 g, 74%). 1H NMR (400 MHz, CDCl3) δ 0.04 (6H, s), 0.87 (9H, m), 2.80 (1H, s), 3.57-3.61 (2H, m), 3.67-3.71 (2H, m), 4.57-4.64 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08071585B2 |
|---|
| Source dataset | uspto-grants-2011_12 |
|---|
| ORD ID | ord-60a0f31b4a2f49388c0670a361b4eb0d |
|---|
| Source note | uspto-grants-2011_12 |
|---|