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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376675Generated: October 31, 2026

Sodium hydride → Tetrakis-[(3-methyl-3-oxetanyl)methoxymethyl]methane

https://huagongshe.com/reaction/1376675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPropane, 1,3-dibromo-2,2-bis(bromomethyl)-HCID 76701—
Reactant3-Methyl-3-oxetanemethanolHCID 137837—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductTetrakis-[(3-methyl-3-oxetanyl)methoxymethyl]methaneHCID 5729385121.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (50% dispersion in mineral oil, 16.10 g. 0.33 mol) was washed twice with hexanes and was suspended in 500 mL of DMF. Then, 3-hydroxymethyl-3-methyloxetane (34.2 g, 0.33 mol) was added dropwise over 45 min while hydrogen gas was evolved and a beige solid precipitated. The mixture was stirred for 30 min and a solution of tetrakis-(bromomethyl)methane (25.0 g, 0.0645 mol) in 250 mL of DMF was added. The mixture was heated to 100° C. for 64 h when 1H NMR analysis of an aliquot showed that the starting halide had been consumed. The mixture was poured into 500 mL of water and extracted with three portions of 200 mL of methylene chloride. The combined organic extracts were washed with 3 portions of 200 mL of water, dried over magnesium sulfate, and evaporated to give an oil. The oil was cooled to -15° C. for 24 h, and the solid that formed was triturated with ether, filtered, and recrystallized from ethanol to give 6.15 g (21.3%) of tetrakis-[(3-methyl-3-oxetanyl)methoxymethyl]methane, mp 108.5°-109.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663289
Source datasetuspto-grants-1997_09
ORD IDord-453d3aef276040608c72772cc9ec2c63
Source noteuspto-grants-1997_09