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HRID 963183作成日:2026年10月26日

Hydrochloric Acid → 3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehyde

https://huagongshe.com/reaction/963183

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物FormaldehydeHCID 712—
反応物Ethyl BromideHCID 6332—
反応物HexamethylphosphoramideHCID 12679—
反応物MagnesiumHCID 5462224—
反応物17-Methylene-estra-1,3,5(10)-trien-3-olHCID 14458552—
溶媒BenzeneHCID 241—
溶媒TetrahydrofuranHCID 8028—
生成物3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehydeHCID 5427244978.2%

反応手順

To a suspension of magnesium (0.365 g, 15 mmol) in THF (3.0 mL) was added bromoethane (1.5 mL, 20 mmol) dissolved in THF (3.0 mL) at room temperature. 17-Methyleneestra-1,3,5(10)-trien-3-ol (19, 0.805 g, 3.0 mmol) dissolved in THF (7.5 mL) was added to the reaction mixture, and stirring continued for 30 min. The solvent was removed at reduced pressure, and to the residue were added benzene (35 mL), hexamethylphosphoric triamide (1.4 mL, 7.5 mmol) and paraformaldehyde (0.630 g). Stirring was continued for 6 h at 80° C. After the reaction mixture was cooled to room temperature, 5N HCl (15 mL) was added and the mixture extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:AcOEt (10:1→3:1, v/v) to afford 0.695 g of 23 (78% yield), m.p. 128°-130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05763432
出典データセットuspto-grants-1998_06
ORD IDord-eebcbbfc98aa4b43a61a7b9480b666ca
出典メモuspto-grants-1998_06