HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375242Generated: October 30, 2026
Dimethylformamide → 3-(Tetradecyloxy)-1,2-propanediol
https://huagongshe.com/reaction/375242
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Solketal | HCID 7528 | — |
| Reactant | Myristyl bromide | HCID 8208 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Tetradecyloxy)-1,2-propanediol | HCID 64674 | 4% |
Reaction Steps
To a mixture of Solketal (66.1 g, 0.5 mol), 1-bromotetradecane (159.4 g, 0.575 mol), and DMF (800 ml) was added 60% NaH (26.0 g, 0.65 mol) in oil dispersion in 3 portions for 1 hr. The mixture was stirred at room temperature for 1 day and methanol (20 ml) was added to destroy the excess NaH. This was then poured into 1500 ml of ice-water and the aqueous layer was extracted with hexanes (2000 ml). The combined organic layers were evaporated to dryness and the oily residue was refluxed in 10% HCl/methanol (conc. HCl, 250 ml and methanol, 675 ml) for 30 min followed by stirring at room temperature overnight. The white flaky solid was filtered and washed with methanol (122 g). The additional product was obtained from the filtrate (5.7 g); Total 127.7 g (88.5%). The crude product was recrystallized from diethyl ether; Yield 99.7 g (69.1%), mp 57°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484911 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-c5d19bf1a64a48dca797660e1d22a0c1 |
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| Source note | uspto-grants-1996_01 |
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