HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348917Generated: October 30, 2026
Lithium Hexamethyldisilazide → HCID 60099787, compound
https://huagongshe.com/reaction/1348917
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone | HCID 4679494 | — |
| Reactant | Ethanedioic acid, monoethyl ester | HCID 21943339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 60099787 | HCID 60099787 | 93.5% |
Reaction Steps
To 6-hydroxy-1-tetralone (10.4 g, 0.064 mol) and ethyl oxalate (17.4 mL, 0.128 mol) in THF (100 mL) was added dropwise lithium bis(trimethylsilyl)amide (1M in THF, 130 mL). The slurry was stirred overnight and a solid was filtered. The solid was dissolved in water and made acidic to pH 2.5 with 3 N HCl, precipitating a waxy solid. The waxy solid was extracted into EtOAc, dried (MgSO4), and concentrated in vacuo leaving a dark solid (15.7 g). The solid was purified by chromatography on silica gel, eluting with 15% EtOAc/hexanes to give a yellow solid (5.9 g). The solid was recrystallized from EtOAc/hexanes to give the product as a yellow solid, 3.7 g (22% yield). FABHRMS m/z 263.0925 (M+H, C14H15O5 requires 263.0919). 1H NMR (CDCl3/300 MHz) 7.93 (d, 1H); 6.80 (d of d, 1H); 6.68 (s, 1H); 5.72 (s, 1H); 4.39 (q, 2H); 3.00-2.75 (m, 4H); 1.40 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211597B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-9c3169ac99e146cf99bcd5e0fb1b396f |
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| Source note | uspto-grants-2007_05 |
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