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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844243Generated: October 30, 2026

Lithium borohydride → tert-Butyl N-[(1R,2S)-rel-2-(4-hydroxyphenyl)cyclopropyl]carbamate

https://huagongshe.com/reaction/1844243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantTert-butyl(trans)-2-[4-(allyloxy)phenyl]cyclopropylcarbamateHCID 86672577—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl N-[(1R,2S)-rel-2-(4-hydroxyphenyl)cyclopropyl]carbamateHCID 8667257690%

Reaction Steps

LiBH4 (0.34 g, 15.54 mmol) was added to a solution of Pd(PPh3)4 (0.15 g, 0.13 mmol) and tert-butyl(trans)-2-[4-(allyloxy)phenyl]cyclopropylcarbamate (Intermediate I, 0.75 g, 2.59 mmol) in dry THF (20 mL) and stirred at room temperature for 1 h. After removal of the solvent, the residue was dissolved in EtOAc (25 mL), acidified with HCl (10% aqueous solution, 2 mL), and washed with water (25 mL) and brine (25 mL). The organic layer was dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residue was purified by column chromatography on silica gel (10%-20% EtOAc/Hexanes), affording 0.58 g of tert-butyl(trans)-2-(4-hydroxyphenyl)cyclopropylcarbamate [Rf=0.3 (30% EtOAc/Hexanes), pale yellow foam, 90% yield].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946296B2
Source datasetuspto-grants-2015_02
ORD IDord-7efc1b8a183d4426bc66494227fa2af6
Source noteuspto-grants-2015_02