HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005006Generated: November 1, 2026
(Diethylamino)sulfur trifluoride → HCID 53985269, compound
https://huagongshe.com/reaction/1005006
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | tert-butyl (3RS,4RS)-3-(4-benzyloxy-naphthalen-2-ylmethoxy)-4-(3-hydroxymethyl-phenyl)-piperidine-1-carboxylate | HCID 54536116 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53985269 | HCID 53985269 | 101.6% |
Reaction Steps
A solution of 18 mg (0.106 mmol) of diethylamino-sulphur trifluoride (DAST) in 1 ml of methylene chloride was cooled to -65° C. and a solution of 56 mg (0.101 mmol) of tert-butyl (3RS,4RS)-3-(4-benzyloxy-naphthalen-2-ylmethoxy)-4-(3-hydroxymethyl-phenyl)-piperidine-1-carboxylate in 1 ml of methylene chloride was added dropwise thereto at -60° C. to -65° C. within 3 minutes. The resulting yellow solution was warmed to room temperature and stirred for one hour. Subsequently, the mixture was partitioned between methylene chloride and 5% sodium hydrogen carbonate solution, the organic phase was dried over magnesium sulphate and finally the solvent was distilled off under reduced pressure. There were obtained 57 mg of crude tert-butyl (3RS,4RS)-3-(4-benzyloxy-naphthalen-2-ylmethoxy)-4-(3-fluoromethyl-phenyl)-piperidine-1-carboxylate, which was used in the next step without further purification and characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051712 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-e1c20ddf1e87465b8aa418e8b9b8386c |
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| Source note | uspto-grants-2000_04 |
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