참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclohexanemethanol | HCID 7507 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | 4-Bromo-2-thiophenecarboxylic Acid | HCID 610409 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Cyclohexylmethyl 4-bromothiophene-2-carboxylate | HCID 86694606 | — |
반응 단계
A solution of oxalyl chloride (1.4 mL, 16.1 mmol) in anhydrous CH2Cl2 (10 mL) was added dropwise to a solution of 4-bromothiophene-2-carboxylic acid (3.08 g, 14.9 mmol) and DMF (0.2 mL) in anhydrous CH2Cl2 (40 mL) over 30 mins. The reaction mixture was stirred at room temperature for 35 min then concentrated under reduced pressure. CH2Cl2 (30 mL) was added to the residue followed by cyclohexylmethanol (1.9 mL, 15.44 mmol) and Et3N (2.5 mL, 17.94 mmol). The reaction mixture was stirred at room temperature overnight and partitioned between EtOAc and aqueous 25% NH4Cl. Organic layer was washed with brine, concentrated under reduced pressure and purified by flash chromatography (2%-20% EtOAc—hexanes gradient) to give cyclohexylmethyl 4-bromothiophene-2-carboxylate as a colorless oil which was directly used in the next step. Yield (3.61 g, 80%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447078B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-d94794a3cec146f9bc1c9a5269329a91 |
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| 출처 메모 | uspto-grants-2016_09 |
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