HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386679Generated: November 1, 2026
Sodium bis(trimethylsilyl)amide → HCID 76477614, compound
https://huagongshe.com/reaction/1386679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 54177953 | HCID 54177953 | — |
| Reactant | HCID 57250465 | HCID 57250465 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 76477614 | HCID 76477614 | 48.7% |
Reaction Steps
A solution of 450 mg (1.81 mmol) of cyclopentylacetic acid, 4-(methoxy)benzyl ester (from EXAMPLE 15, Step A) in 6 mL of THF was added to 2.15 mL of 1.0 M sodium bis(trimethylsilyl)amide solution in THF at −78° C. and the resulting mixture was stirred cold for 15 min. A solution of 700 mg (2.67 mmol) of (benzenesulfonyl)phenyloxaziridine in 3 mL of THF was the added and the resulting mixture was stirred at −78° C. for 1 h. The reaction was quenched with sat'd NH4Cl and warmed to rt. The mixture was concentrated and the residue was dissolved in 100 mL of ether and washed with 100 mL of sat'd NaCl. The phases were separated and the aqueous layer was extracted with 100 mL of ether. The combined organic layers were dried over MgSO4 and concentrated. Flash chromatography on silica gel using 9:1 v/v hexanes/EtOAc as the eluant afforded 233 mg (48%) of the title compound: RF: 0.37 (4:1 v/v hexanes/EtOAc); 1H NMR (300 MHz) δ 1.36-1.69 (m, 8H), 2.22 (m, 11H), 3.81 (s, 3H), 4.14 (d, J=4.9, 11H), 5.14 (ABq, J=11.8, 2H), 6.89 (d, J=8.8, 2H), 7.29 (d, J=8.8, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06265434B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-bca92db97c76495fbce48eec229926de |
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| Source note | uspto-grants-2001_07 |
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