HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752020Generated: October 28, 2026
Dichloromethane → 4-[2-(Toluene-4-sulfonyloxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester
https://huagongshe.com/reaction/1752020
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Tert-Butyl 4-(2-(hydroxymethyl)phenyl)piperidine-1-carboxylate | HCID 57774474 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[2-(Toluene-4-sulfonyloxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester | HCID 46212988 | 112.2% |
Reaction Steps
4-(2-Hydroxymethylphenyl)piperidine-1-carboxylic acid t-butyl ester (0.4 g, 1.0 mmol, 1.0 eq.) and triethylenediamine (220 mg, 2.0 mmol, 1.4 eq.) were dissolved in DCM (11 mL, 170 mmol). The mixture was cooled at 0° C. under nitrogen, TsCl (290 mg, 1.5 mmol, 1.1 eq.) was added, and the mixture was stirred at 0° C. for an additional 60 minutes. The mixture was diluted with EtOAc (50 mL) and washed with water (2×25 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated by rotary evaporation to yield the title compound (500 mg), which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09162982B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-cfec62ab06364c2994b8ee833bc0bfde |
|---|
| Source note | uspto-grants-2015_10 |
|---|