HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263833Generated: October 26, 2026
1-Bromohexadecane → HCID 14350902, compound
https://huagongshe.com/reaction/263833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromohexadecane | HCID 8213 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Trityloxypropane-1,2-diol | HCID 2882827 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14350902 | HCID 14350902 | 68.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05645883 |
|---|
| Source dataset | uspto-grants-1997_07 |
|---|
| ORD ID | ord-01fff633c6774e4eb8c309ed33313eba |
|---|
| Source note | uspto-grants-1997_07 |
|---|