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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13223Generated: October 25, 2026

Isopropanol → t-Butyl (1R,2R)-1-(2,3-dihydrobenzofuran-6-yl)-1-hydroxypropan-2-ylcarbamate

https://huagongshe.com/reaction/13223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantAluminum tri-iso-propoxideHCID 16685055—
Reactant(R)-t-butyl 1-(2,3-dihydrobenzofuran-6-yl)-1-oxopropan-2-ylcarbamateHCID 59339724—
SolventTolueneHCID 1140—
Productt-Butyl (1R,2R)-1-(2,3-dihydrobenzofuran-6-yl)-1-hydroxypropan-2-ylcarbamateHCID 5933979671%

Reaction Conditions

Temperature50 °C

Reaction Steps

(R)-t-butyl 1-(2,3-dihydrobenzofuran-6-yl)-1-oxopropan-2-ylcarbamate (306d, 2.21 g, 7.59 mmol) was dissolved in propan-2-ol (6.35 mL, 83.4 mmol) and toluene (10 mL). Al(OiPr)3 (0.310 g, 1.52 mmol) was added, and the reaction vessel was capped and flushed with argon. The mixture was stirred at 50° C. overnight. Then another portion of Al(OiPr)3 (330 mg) was added, and stirring was continued for 5 h. The mixture was cooled to r.t., and partitioned between aq. HCl (1N, 25 ml) and ethyl acetate (80 ml). The organic layer was separated and dried. The solvent was removed in vacuo and purified by flash chromatography on silica gel with n-heptane/ethyl acetate (6:4) to give 1.58 g (71%) of subtitle compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728030B2
Source datasetuspto-grants-2010_06
ORD IDord-67a5a537560240f09f61349ff310076a
Source noteuspto-grants-2010_06