Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891049Generated: October 25, 2026

Ytterbium → tert-Butyl piperazine-1-carboxylate

https://huagongshe.com/reaction/891049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantYtterbiumHCID 23992—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 23598944HCID 23598944—
SolventDichloromethaneHCID 6344—
Producttert-Butyl piperazine-1-carboxylateHCID 143452—
Product(2S)-1-(2-methylbenzothiazol-5-yloxy)butan-2-olHCID 69622255—

Reaction Steps

To a solution of 5-[((2S)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 (2S)-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 numberUS07001909B2
Source datasetuspto-grants-2006_02
ORD IDord-d33019e973ea4497a1d6185fb865729b
Source noteuspto-grants-2006_02