HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818635Generated: November 1, 2026
tert-Butyl acetate → HCID 91509324, compound
https://huagongshe.com/reaction/1818635
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 87416753 | HCID 87416753 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 91509324 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598398B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-dcb5188314dc41cb982601a534ea500f |
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| Source note | uspto-grants-2009_10 |
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