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HRID 2757作成日:2026年10月26日

Hydrochloric Acid → 5-Iodo-2-(2-methoxy-ethoxymethoxy)-benzyl alcohol

https://huagongshe.com/reaction/2757

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Sodium hydrideHCID 24758—
反応物5-IodosalicylaldehydeHCID 252612—
反応物Sodium borohydrideHCID 4311764—
反応物Methoxyethoxylmethoxyl chlorideHCID 19350948—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物5-Iodo-2-(2-methoxy-ethoxymethoxy)-benzyl alcoholHCID 5371346880.4%

反応条件

温度-15 °C

反応手順

To a solution of sodium hydride (1.2 g of a 60% mineral oil dispersion, 52 mmol) in 25 mL of THF at 0° C., is added 2-hydroxy-5-iodo-benzaldehyde (7.0 g, 28 mmol). To the resulting solution is added 2-methoxy-ethoxymethoxy chloride (3.4 mL, 30 mmol) and 4 mL of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone. The solution is allowed to warm to ambient temperatures. After 45 min., the solution is cooled to -15° C. and 6 mL of a 2M solution of sodium borohydride in THF is added. The solution is stirred for 10 min. After this time, 24 mL of a 2M HCl solution in water is added. The resulting solution is diluted with ether, washed with water and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The resulting crude material is purified by column chromatography eluting with 40% EtOAc/hexanes to give the title compound (7.6 g, 22.5 mmol) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731315
出典データセットuspto-grants-1998_03
ORD IDord-2272a341dfe943cb9a6785a30ad21c5c
出典メモuspto-grants-1998_03