Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263833Generated: October 26, 2026

1-Bromohexadecane → HCID 14350902, compound

https://huagongshe.com/reaction/263833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexadecaneHCID 8213—
ReactantSodium hydrideHCID 24758—
Reactant3-Trityloxypropane-1,2-diolHCID 2882827—
SolventDimethylformamideHCID 6228—
ProductHCID 14350902HCID 1435090268.3%

Reaction Steps

1H-nmr (200 MHz, CDCl3), 3.21 (2H, m), 3.65 (2H, m), 3.85 (1H, m), 7.4 (15H, m). ##STR17## Sodium hydride (prewashed with hexane, 60% oil dispersion, 0.79 g, 32.89 mmol) was stirred in dry dimethyl formamide (50 ml) under a stream of nitrogen. 1-trityl glycerol (5.0 g, 14.95 mmol) in dry dimethyl formamide (50 ml) was added carefully. The reaction was stirred at room temperature for 30 minutes before 1-bromohexadecane (9.13 g, 29.90 mmol) was added and the reaction was stirred at room temperature under a nitrogen atmosphere for 12 hours. The reaction mixture was carefully partitioned between dichloromethane (100 ml) and water (100 ml×3). The organic layer was washed successively with saturated NaHCO3 (100 ml) and brine (100 ml), dried over sodium sulphate and evaporated to yield the crude product, which was purified by column chromatography eluting with (40-60) light petroleum: ethyl acetate (230:20). Fractions containing product were evaporated to dryness to give 1,2-dihexadecyl-3-trityl glycerol (8.00 g, 10.21 mmol) 68% yield

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05645883
Source datasetuspto-grants-1997_07
ORD IDord-01fff633c6774e4eb8c309ed33313eba
Source noteuspto-grants-1997_07