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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2757생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2757

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물5-IodosalicylaldehydeHCID 252612—
반응물Sodium borohydrideHCID 4311764—
반응물Methoxyethoxylmethoxyl chlorideHCID 19350948—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물5-Iodo-2-(2-methoxy-ethoxymethoxy)-benzyl alcoholHCID 5371346880.4%

반응 조건

온도-15 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731315
출처 데이터셋uspto-grants-1998_03
ORD IDord-2272a341dfe943cb9a6785a30ad21c5c
출처 메모uspto-grants-1998_03