참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | 4-Methoxy-2-methylbenzoic acid | HCID 597216 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-one | HCID 12401182 | — |
반응 단계
A 1.6M solution of n-butyllithium in hexane (145.9 mL) was added dropwise at −78° C. to a solution of diisopropylamine (33.5 mL) in dry THF (190 mL). Then the reaction mixture was warmed to room temperature for 5 min, and then cooled again to −78° C., and a solution of 4-methoxy-2-methylbenzoic acid in dry THF (210 mL) was added dropwise. After stirring at this temperature for 10 min, paraformaldehyde (7 g) was added. Then the reaction mixture was allowed to return to room temperature and it was stirred at this temperature for 4 h. Water was added to the reaction mixture, then the THF was removed in vacuum and then the aqueous phase was extracted with diethyl ether. The aqueous phase was acidified with conc. HCl, the precipitate obtained was filtered off and washed with water several times. In this way the product was obtained with molecular weight 178.06 (C10H10O3); MS (ESI): 179 (M+H+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822495B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-7fc365ab56c64ed2a4187612a70af1c8 |
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| 출처 메모 | uspto-grants-2014_09 |
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