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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827876Generated: November 2, 2026

Ytterbium → tert-Butyl piperazine-1-carboxylate

https://huagongshe.com/reaction/1827876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantYtterbiumHCID 23992—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-(((R)-oxiran-2-yl)methoxy)-2-methylbenzo[d]thiazoleHCID 21023606—
SolventDichloromethaneHCID 6344—
Producttert-Butyl piperazine-1-carboxylateHCID 143452—
ProductHCID 69600520HCID 69600520—

Reaction Steps

To a solution of 5-[((2R)oxiran-2-yl)methoxy]-2-methylbenzothiazole, a compound of formula (3) (6.2 g, 28 mmol), and tert-butyl 1-piperazinecarboxylate, a compound of formula (4) (5.7 g, 31 mmol), in methylene chloride (200 ml), was added ytterbium (111) trifluoromethanesulfonate (1.73 g, 28 mmol). The resulting solution was allowed to stir at room temperature overnight. The solvent was evaporated (in vacuo), to yield a semi-solid, which was chromatographed on silica gel, eluting with 5% methanol/methylene chloride, to yield (2R)-1-(2-methylbenzothiazol-5-yloxy)butan-2-ol, tert butyl piperazinecarboxylate as a clear oil (9.5 g, 23 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056924B2
Source datasetuspto-grants-2006_06
ORD IDord-cf496e8b3a1f418e8229ac4f69409dc5
Source noteuspto-grants-2006_06