HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82961Generated: October 25, 2026
1-Pentanethiol → 1-(Diphenylmethyl)-3-(pentylthio)azetidine
https://huagongshe.com/reaction/82961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pentanethiol | HCID 8067 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(Diphenylmethyl)-3-(pentylthio)azetidine | HCID 67154644 | 96% |
Reaction Steps
To a solution of pentanethiol (248 μL, 2.0 mmol) in DMSO (2.5 mL) at 0° C. under nitrogen was added NaH (60% in oil, 80 mg, 2.0 mmol). The suspension was stirred for 0.5 h at 0° C. then treated with 1-(diphenylmethyl)azetidin-3-yl methanesulfonate (317 mg, 1.0 mmol; which may be prepared as described in Step 1) and the mixture allowed to warm to room temperature overnight. Saturated NaHCO3 (5 mL) was added and the mixture was extracted with diethyl ether. The organic layer was separated from the aqueous and the organic washed with brine, dried over Na2SO4 and concentrated to give the product (312 mg, 96%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08846711B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-9db5e2616292487cb7e0fd504a634062 |
|---|
| Source note | uspto-grants-2014_09 |
|---|