Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513105Generated: October 31, 2026

2-Chloromethyl 2-(trimethylsilyl)ethyl ether → HCID 68354670, compound

https://huagongshe.com/reaction/513105

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-tert-Butyl 2-methyl morpholine-2,4-dicarboxylateHCID 58817474—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68354670HCID 6835467080%

Reaction Conditions

Temperature-78 °C

Reaction Steps

E1 (5.0 g 20.39 mmol) was dissolved in THF (45 mL) and cooled to −78° C. LHMDS (1 M in hexane/ethylbenzene) (40.8 mL, 40.8 mmol) was added in 30 minutes and the solution was stirred for 35 min at −78° C. (2-(Chloromethoxy)ethyl)trimethylsilane (10.02 mL, 56.5 mmol) was added and the reaction mixture was allowed to warm to room temperature overnight. The reaction mixture was quenched with saturated NH4Cl and extracted twice with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by flash column chromatography (heptane:EtOAc=100:0 to 70:30) yielding the title compound (6.09 g, 80%). 1H NMR (400 MHz, CDCl3, 300K): δ 0.00 (3H, s), 0.92 (2H, t, J=7.5 Hz), 1.47 (9H, s), 3.02 (2H, d, J=13.3 Hz), 3.55 (4H, m), 3.78 (3H, s), 3.83 (3H, m), 4.34 (1H, d, J=13.3 Hz). MS (ES) C17H33NO6Si requires: 375. found: 398.2 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102676B2
Source datasetuspto-grants-2015_08
ORD IDord-78b9975fc24741b5b6ee981dc9c747b5
Source noteuspto-grants-2015_08