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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451746Generated: October 30, 2026

Tetrahydrofuran → HCID 178484174, compound

https://huagongshe.com/reaction/451746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantFluoride IonHCID 28179—
ReactantPerfluoro-1-butanesulfonyl fluorideHCID 67814—
ReactantHCID 178484177HCID 178484177—
ProductHCID 178484174HCID 17848417420%

Reaction Steps

A mixture of benzyl (S)-2-(t-butoxycarbonylamino)-3-(cis-4-hydroxycyclohexyl)-propyl(methyl)carbamate (1 g, 2.38 mmol), base Et3N (5 mL, 28 mmol), a fluoride source NEt3(HF)3 (1.9 mL, 9.52 mmol) and perfluorobutanesulfonyl fluoride (2.1 mL, 9.52 mmol) were stirred in THF (24 mL, 1 mmol/10 mL) in a capped vial or flask at 50° C. until LC revealed complete conversion. The reaction mixture was quenched with water and extracted with EtOAc (2×100 mL), dried over MgSO4, and evaporated. The residue was then purified by preparative HPLC to give benzyl (S)-2-(t-butoxycarbonylamino)-3-(trans-4-fluorocyclohexyl)propyl-(methyl)carbamate (200 mg, 20%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487108B2
Source datasetuspto-grants-2013_07
ORD IDord-985ec7b48f544c9cb7320a395382abcf
Source noteuspto-grants-2013_07