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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111750Generated: November 1, 2026

Hydrogen Peroxide → HCID 58817704, compound

https://huagongshe.com/reaction/2111750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 49760093HCID 49760093—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58817704HCID 5881770459%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidine-1-carboxylic acid tert-butyl ester (1.00 g, 3.13 mmol) in dry tetrahydrofuran (31.3 mL) cooled to −78° C. was added lithium diisopropylamide (1.72 mL, 3.35 mmoles). The resulting solution was stirred at −78° C. for 2 hours when trimethylborate (0.44 mL, 3.84 mmoles) was added. The resulting solution was stirred at −78° C. for 1 hour then was allowed to warm to room temperature over 3 hours when hydrogen peroxide (2.00 mL) and acetic acid (1.00 mL) were added. The resulting mixture was stirred at room temperature overnight when the mixture was quenched with saturated NH4Claq (20 mL) and 10% HClaq (20 mL). The resulting mixture was extracted with CH2Cl2 (4×50 mL). The combined extracts were washed with brine (50 mL), dried (MgSO4), filtered and evaporated. The residue was separated via column chromatography (1:1; Et2O/Pet. ether) yielding 0.619 g (59%) of the phenol as a white, crystalline solid, mp 169-170° C. Analysis calculated for C17H21N2FO4; 60.70% C, 6.29% H, 8.33% N. Found: 60.72% C, 6.15% H, 8.22% N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521445B2
Source datasetuspto-grants-2009_04
ORD IDord-dc0233cc1ca644a88a03e9914d5d908f
Source noteuspto-grants-2009_04