Sodium hydride → 6-(7-Hydroxyheptyl)-7-(6-methoxy-3-oxohex-1-enyl)-1,4-dioxaspiro[4,4]nonane

A solution of dimethyl 5-methoxy-2-oxopentylphosphonate (5.3 g.) in tetrahydrofuran (19 ml.) was added to a stirred suspension of sodium hydride (0.39 g.) in tetrahydrofuran (140 ml.). The mixture was stirred at room temperature until the evolution of hydrogen had ceased, then treated dropwise with a solution of 7-formyl-6-(7-hydroxyheptyl)-1,4-dioxaspiro[4,4]nonane [4.8 g.; prepared as described in Example 1(iv)] in tetrahydrofuran (47 ml.) and stirred for a further 2 hours. The mixture was acidified to pH 4 by the addition of glacial acetic acid, the solvents were removed in vacuo and diethyl ether was added to the residue. The solid was filtered off and the filtrate was washed with aqueous sodium carbonate, dried over anhydrous sodium sulphate, and evaporated to dryness, to give 6-(7-hydroxyheptyl)-7-(6-methoxy-3-oxohex-1-enyl)-1,4-dioxaspiro[4,4]nonane (6.4 g.), νmax 1620 cm-1, 1660 cm-1.

1. customthe solvents were removed in vacuo and diethyl ether
2. additionwas added to the residue
3. filtrationThe solid was filtered off
4. washthe filtrate was washed with aqueous sodium carbonate
5. dry with materialdried over anhydrous sodium sulphate
6. customevaporated to dryness

ORDレコード

ord-1e0b4b365bad4e5eb65c81d245972d96

出典データセット

uspto-grants-1977_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04036872