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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418368Generated: October 29, 2026

Hexamethyldisilazane → HCID 59164836, compound

https://huagongshe.com/reaction/418368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 59164823HCID 59164823—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59164836HCID 5916483687.1%

Reaction Steps

To a solution of (5R)-1-{[(1,1-dimethylethyl)oxy]carbonyl}-5-{4-[(phenylmethyl)oxy]phenyl}-L-proline (1.44 g, 3.62 mmol) in dry DMF (20 ml) were added DIPEA (1.26 ml, 7.24 mmol), then TBTU (1.23 g, 3.98 mmol) and after 20 minutes, 1,1,1,3,3,3-hexamethyldisilazane (1.15 ml, 5.43 mmol). The reaction mixture was stirred at room temperature for 2 h, then it was treated with aqueous 5% NaHCO3 solution (30 ml) and stirred for further 30 minutes. The resulting mixture was diluted with water and extracted with ethyl acetate. The organic phase was then washed twice with brine/ice, dried over Na2 SO4 and evaporated to give a colourless oil. This crude material was purified by chromatography on silica gel eluting with cyclohexane/ethyl acetate (7:3 to 5:5) to afford the title compound (1.25 g, 87%); Rt (HPLC): 5.51 min; Rf (cyclohexane:ethyl acetate=1:1): 0.29. MS: (ES/+) m/z: 419 [M+Na+]; C23H28N2O4 requires 396.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093268B2
Source datasetuspto-grants-2012_01
ORD IDord-955bbf4f1f6d476ea15b5dfb16698b5c
Source noteuspto-grants-2012_01