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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818635Generated: November 1, 2026

tert-Butyl acetate → HCID 91509324, compound

https://huagongshe.com/reaction/1818635

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 87416753HCID 87416753—
SolventTetrahydrofuranHCID 8028—
ProductHCID 91509324HCID 91509324—

Reaction Steps

To a cooled (−78° C.) solution of LHMDS (4.5 mL, 1.0 M in THF, 4.5 mmol) in THF (13 mL) was added tert-butyl acetate (0.600 mL, 4.46 mmol), dropwise. After 30 min, a solution of the title compound of Example 13 Step A (620 mg, 1.50 mmol) in THF (4 mL) was added, and the mixture was held at −78° C. for 30 min, then was placed in a 0° C. bath. After 1.5 h, the reaction mixture was poured into sat. aq. NaHCO3 and extracted twice with EtOAc. The combined organic phases were concentrated in vacuo. Purification by flash chromatography on silica gel (0 to 30%, then 30 to 100% hexanes in EtOAc) afforded the title compound: LCMS B, tr=2.90 min, m/z 432.0 [M−tBu+H]+; 1H NMR (500 MHz, CDCl3) δ 7.79 (d, J=8.5 Hz, 2H), 7.64 (s, 1H), 7.46 (s, 1H), 7.44 (d, J=8.5 Hz, 2H), 7.21 (dd, J=9.0, 2.0 Hz, 1H), 7.11 (d, J=9.0 Hz, 1H), 3.85 (s, 2H), 1.46 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598398B2
Source datasetuspto-grants-2009_10
ORD IDord-dcb5188314dc41cb982601a534ea500f
Source noteuspto-grants-2009_10