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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025321Generated: October 26, 2026

Benzoxazole → tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamate

https://huagongshe.com/reaction/1025321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoxazoleHCID 9228—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamateHCID 11522383—

Reaction Conditions

Temperature-5 °C

Reaction Steps

Under an atmosphere of argon, benzo[d]oxazole (5 g, 42.0 mmol, Eq: 1.00) was combined with THF (100 ml) to give a light yellow solution. At −5° C. isopropylmagnesium chloride 2M in THF (21.0 ml, 42.0 mmol, Eq: 1.00) was added dropwise. The reaction was stirred for 1.5 h at −5° C. Then (S)-tert-butyl 1-oxobutan-2-ylcarbamate (4.72 g, 25.2 mmol, Eq: 0.6) diluted in 20 ml THF was added. The reaction was stirred overnight at RT. Satd. ammoniumchloride solution (6 ml) was added to the reaction. The THF was evaporated under vacuum. The reaction mixture was poured into 50 ml H2O and extracted with ethyl acetate (2×100 ml). The crude material was purified by flash chromatography (silica gel, 20 g, 0% to 40% ethyl acetate in heptane). The title compound was obtained as a brown gum (5.08 g, 39.5%, MS (m/e)=307.2 [M+H+]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729061B2
Source datasetuspto-grants-2014_05
ORD IDord-545695dd0df944b9b559205a855afc46
Source noteuspto-grants-2014_05