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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341515Generated: November 1, 2026

Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate → HCID 57898964, compound

https://huagongshe.com/reaction/341515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—
Reactant1-Propanethiol, sodium salt (1:1)HCID 4681725—
ReactantHCID 86710527HCID 86710527—
ProductHCID 57898964HCID 5789896460%

Reaction Steps

tert-Butyl 4-[(propan-2-ylsulfanyl)methyl]piperidine-1-carboxylate was prepared from tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate (Intermediate 181, 0.320 g, 1.091 mmol) and sodium propanethiolate (0.161 g, 1.636 mmol) according to the method described for Intermediate 183 to afford the title compound (0.180 g, 60%). Method B HPLC-MS: MH+ requires m/z=274 Found: m/z=218 (M-tert-Bu), Rt=2.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-d8ff25f5156e4278983270ba225be002
Source noteuspto-grants-2014_11