참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Thioglycolic Acid | HCID 1133 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 4-(Chloromethyl)-2-nitroanisole | HCID 80785 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | HCID 178490206 | HCID 178490206 | 103.6% |
반응 단계
To a cold solution of sodium hydroxide (9.75 g, 240 mmol) in methanol (200 mL), was added thioglycollic acid (11.25 g, 120 mmol) slowly over 30 min. Sodium thioglycollate precipitated and was redissolved by stirring and warming the mixture. The sodium thioglycollate solution was then cooled to room temperature and 4-methoxy-3-nitrobenzyl chloride (30.0 g, 120 mmol) was added in portions to reduce the intensity of exothermic reaction. The resulting mixture was heated to reflux temperature and maintained at reflux temperature for 4 h. The heated mixture was then cooled and poured onto crushed ice (1 kg) containing hydrochloric acid (50 mL). A precipitate formed. The precipitate was separated by filtration, washed with ice cold water and dried under vacuum to yield 30 g (95% yield) of the desired 4-methoxy-3-nitrobenzylthioacetic acid product. m.p. 130-132° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08106033B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-bf0401ec1ff24fe39ccaf024f80df387 |
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| 출처 메모 | uspto-grants-2012_01 |
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