Sodium Hydroxide → HCID 86734013, compound

A mixture of 0.194 g. (0.007952 mole) of sodium hydride (free of mineral oil) and 5.5 ml. of dimethylsulfoxide is heated to 70°C. until gas evolution ceases under a nitrogen atmosphere. The resulting solution is cooled below room temperature and treated with a solution of 1.400 g. (0.00316 mole) of 4-carboxybutyltriphenyl phosphonium bromide [E. J. Corey et al., J. Am. Chem. Soc., 91, 5675 (1969)] in 6 ml. of dimethylsulfoxide. To the resulting red solution is added 0.738 g. (0.00263 mole) of 2-(formylmethyl)-3-(1-trans-octenyl)-1,1-dioxolano cyclopentane in 2 ml. of dimethylsulfoxide and the mixture is stirred at room temperature for 2.25 hours. The mixture is poured into ice water, sodium hydroxide solution is added to pH 12, and the neutral materials are extracted with diethyl ether. The basic phase is acidified with dilute hydrochloric acid and is extracted with diethyl ether. The organic phase is washed with water and saturated brine, dried (Na2SO4), and evaporated to a semicrystalline mass. The latter is triturated with hot hexane, the solids are filtered off, and the filtrate is evaporated to yield an oil. IR: 1705, 1040, 970, 722 cm-1.

1. additionA mixture of 0.194 g
2. temperatureThe resulting solution is cooled below room temperature
3. additiontreated with a solution of 1.400 g
4. additionTo the resulting red solution is added 0.738 g
5. additionis added to pH 12
6. extractionthe neutral materials are extracted with diethyl ether
7. extractionis extracted with diethyl ether
8. washThe organic phase is washed with water and saturated brine
9. dry with materialdried (Na2SO4)
10. customevaporated to a semicrystalline mass
11. customThe latter is triturated with hot hexane
12. filtrationthe solids are filtered off
13. customthe filtrate is evaporated
14. customto yield an oil

ORD record

ord-d574bb5bab04423d90f81dfb99dc3e84

Source dataset

uspto-grants-1976_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US03981868