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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470605Generated: October 25, 2026

Sodium hydride → HCID 136413210, compound

https://huagongshe.com/reaction/470605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic Acid Methyl EsterHCID 67396155—
ReactantHCID 178449909HCID 178449909—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136413210HCID 136413210—

Reaction Steps

A solution of N-hydroxy-butyramidine (0.24 g, 2.34 mmol) in tetrahydrofuran (5 mL) was added slowly into the suspension of 60% sodium hydride (0.14 g, 3.5 mmol) in dry tetrahydrofuran (5 mL) under nitrogen atmosphere at 0° C. to 10° C. The mixture was stirred for 30 min at room temperature. 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid methyl ester (compound of Example 1, Step 1; 0.5 g, 1.18 mmol) in dry tetrahydrofuran (5 mL) was added into the reaction mixture and heated at 60° C. for 8 h. The reaction mixture was cooled at 0° C. and quenched with methanol (2 mL) to destroy excess sodium hydride. The reaction mixture was extracted with ethyl acetate (2×10 mL) and the combined organic layers were washed with water (2×10 mL) followed by brine (10 mL). The organic phase obtained was dried over anhydrous sodium sulphate and concentrated to dryness. The crude product obtained was purified by column chromatography (silica gel, chloroform-methanol) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-4c664d48321d4babab4ca34308e1347e
Source noteuspto-grants-2014_01