Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62771Generated: October 27, 2026

Acetic Acid → HCID 13861701, compound

https://huagongshe.com/reaction/62771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
Reactanttert-Butyl(4-fluorobenzyloxy)dimethylsilaneHCID 13861700—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13861701HCID 1386170159.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

sec-Butyllithium (20.7 mL, 29.0 mmol) was added dropwise to a solution of tert-butyl(4-fluorobenzyloxy)dimethylsilane (2) (6.33 g, 26.3 mmol) in THF (30 mL) over 30 min, at −78° C. Trimethyl borate (2.99 mL, 26.3 mmol) was added dropwise over 30 min while the temperature was maintained at −78° C. The reaction mixture was allowed to warm to 0° C. and AcOH (2.26 mL, 39.5 mmol) was added dropwise, followed by hydrogen peroxide (2.48 mL, 29.0 mmol). The mixture was stirred at 0° C. for 30 min then allowed to warm to RT and stirred for 1 h. The reaction mixture was diluted with diethyl ether (100 mL) and washed with 2M NaOH (100 mL) and brine (100 mL). The organic solution was dried over MgSO4, filtered and the solvent was removed in vacuo to give 5-((tert-butyldimethylsilyloxy)methyl)-2-fluorophenol (3) (4.0 g, 50%) as a colourless oil: m/z 255 [M−H]− (ES−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-e64194a762cc4935b9b6faeb1d5be5fa
Source noteuspto-grants-2016_09