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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387202생성일: 2026년 10월 24일

Hydrochloric Acid → 2,3-Dihydro-1-benzofuran-7-carbaldehyde

https://huagongshe.com/ko/reaction/387202

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Methyl chloroformateHCID 6586—
반응물2,3-Dihydro-1-benzofuran-7-carboxylic acidHCID 2795014—
반응물Sodium borohydrideHCID 4311764—
반응물HCID 178418287HCID 178418287—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2,3-Dihydro-1-benzofuran-7-carbaldehydeHCID 279501860.7%

반응 단계

2,3-Dihydrobenzofuran-7-carboxylic acid (820 mg, 5 mmol) was dissolved in THF (10 mL). To the solution was added TEA (0.7 mL, 5 mmol) and methylchloroformate (0.43 mL, 5 mmol). The solution was stirred for 0.5 hour. The white precipitates were removed by filtration, the filtrate was added to a solution of NaBH4 (437 mg, 12.5 mmol) in H2O (5 mL). The resulting solution was stirred overnight. The reaction mixture was neutralized with 2 M aqueous HCl solution and then extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous Na2SO4 and concentrated in vacuo. The crude alcohol was dissolved in DCM. To the solution was added PCC (1.83 g, 7.5 mmol). The mixture was stirred for 2 hours at room temperature and diluted with diethyl ether, then ether layers were decanted. Combined organic layer was filtered though a layer of Celite®. The filtrate was concentrated to give crude product. The crude was purified from column with 10% EtOAc/hexane to afford 450 mg of 2,3-dihydrobenzofuran-7-carbaldehyde as a slightly yellow solid. HPLC 4.3 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372873B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-538a097432f74bc881d497f121b88a50
출처 메모uspto-grants-2013_02