Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 54177953HCID 54177953—
ReactantHCID 57250465HCID 57250465—
SolventTetrahydrofuranHCID 8028—
ProductHCID 76477614HCID 7647761448.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-bca92db97c76495fbce48eec229926de
Source noteuspto-grants-2001_07