Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Tetraglyme | HCID 8925 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | F5S(CF2)3CO2CH3 | HCID 131717602 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131717601 | HCID 131717601 | — |
Reaction Steps
Sodium borohydride (0.32 g) was added to 25 g tetraglyme with rapid stirring. At room temperature 4.8 g of Cut 2 (b.p. 110°-130° C.) from Example 11, F5S(CF2)3CO2CH3, was added to the sodium borohydride solution over a period of 1.5 hrs. The crude reaction mixture was heated to 47° C. and held at that temperature for one hr. The reaction mixture then was cooled to room temperature and 50 mL water was added. After the water was added, 1 mL of concentrated sulfuric acid was introduced. The reaction mixture was heated to 100° C., at which point an azeotrope of the fluorochemical and water distilled from the reaction mixture. The crude reaction mixture was heated until no more fluorochemical distillate was produced. The water and fluorochemical were phase-separated. A total of 2.2 g crude fluorochemical, a yellow foul-smelling liquid, was collected. GC-mass spectral, IR, and F19 nmr spectral analyses showed the liquid to comprise following composition (in mole %): 90.9% F5S(CF2)3CH2OH, 1.5% F5SCF(CF3)CF2CH2OH, 0.4% F5SCF2CF(CF3)CH2OH, 3.3% F5S(CF2)3CH(OH)2, 3.8% F5S(CF2)3CH(OH)(CH3) or F5S(CF2)3CH(OH)(CH2Rf).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05159105 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-fc54cd6209c642f597c5ce1c812c25d6 |
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| Source note | uspto-grants-1992_10 |
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