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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341553Generated: October 31, 2026

Sodium hydride → HCID 86710527, compound

https://huagongshe.com/reaction/341553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—
Reactant2,2,2-TrifluoroethanethiolHCID 4133924—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86710527HCID 86710527—

Reaction Steps

2,2,2-Trifluoroethane-1-thiol (471 μL, 3.41 mmol) was added dropwise to a suspension of sodium hydride (60% dispersion in mineral oil, 0.065 g, 1.636 mmol) in dry DMF (10 mL) at 0 C and the mixture was stirred for 15 min. A solution of tert-butyl 4-[(methanesulfonyloxy)methyl]piperidine-1-carboxylate (prepared in an analogous manner to Intermediate 181, 1 g, 3.41 mmol) in DMF (5 mL) was added dropwise and the mixture was stirred at room temperature for 5 h. The reaction mixture was diluted with water (50 mL) and extracted with EtOAc (3×50 mL). The combined organic layers were washed with saturated aq. sodium bicarbonate (25 mL) then brine (25 mL), dried over magnesium sulfate and concentrated under reduced pressure to provide the title compound as a light yellow oil (1.13 g, quant.). Method B HPLC-MS: MH+ requires m/z=314 Found: m/z=258 (MH+-tBu), Rt=2.39 min (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-09d437709eb9477594777167d5c87d17
Source noteuspto-grants-2014_11