참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuryl chloride | HCID 24648 | — |
| 반응물 | HCID 22966386 | HCID 22966386 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(Benzyloxy)benzene-1-sulfonyl chloride | HCID 15729649 | — |
반응 단계
Magnesium 3-benzyloxyphenylsulfinate bromide, as described above in Step B, (4.5 g, 14 mmol) was dissolved in dry CH2Cl2 (175 mL) and cooled to 0° C. under argon. Sulfuryl chloride (19 mL of a 1.0 M solution in CH2Cl2, 19 mmol) was added dropwise, and the mixture was stirred for 18 hours at ambient temperature, during which time a precipitate formed. The precipitate was removed by filtration and the filtrate was concentrated under reduced pressure to give the product as a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06441017B1 |
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| 출처 데이터셋 | uspto-grants-2002_08 |
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| ORD ID | ord-973767a9431f4601b10c27bf4cc83112 |
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| 출처 메모 | uspto-grants-2002_08 |
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