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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 250219생성일: 2026년 10월 27일

Hydrochloric Acid → 5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxole

https://huagongshe.com/reaction/250219

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물DichloromethaneHCID 6344—
반응물1,3-Benzodioxole, 5-methyl-HCID 81564—
촉매Tetrabutylammonium BromideHCID 74236—
용매Diethyl EtherHCID 3283—
생성물5-(Chloromethyl)-6-methylbenzo[d][1,3]dioxoleHCID 1055941662%

반응 조건

온도0 °C

반응 단계

At about 0° C., 5-methylbenzo[d][1,3]dioxole (500 mg, 3.68 mmol) and formaldehyde (37% in water, 0.7 mL) were sequentially added to a mixture of dichloromethane (6.8 mL), tetrabutylammonium bromide (80 mg) and concentrated hydrochloric acid (6.5 mL). Under continuous stirring, the mixture was maintained at about 0° C. for about 1 hour and then at ambient temperature for about 4 hours. The mixture was diluted with ether (100 mL). After standard extractive workup, the resulting solid residue was heated with hexanes (100 mL) and the insolubles were removed by filtration. The filtrate was concentrated to give desired product (420 mg, 62%). 1H NMR (300 MHz, CDCl3) δ 6.89 (s, 1H), 6.69 (s, 1H), 5.94 (s, 3H), 4.56 (s, 2H), 2.35 (s, 3H); GC-MS: m/z=184 (MH)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863308B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-b6b6d050f2924effa5aa7dbff1654bc5
출처 메모uspto-grants-2011_01