Aniline → HCID 13564469, 화합물
반응식
[OH:1][C:2]1[C:3]([CH:12]=O)=[CH:4][C:5]2[O:10][CH2:9][CH2:8][CH2:7][C:6]=2[CH:11]=1.[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>CO>[OH:1][C:2]1[C:3]([CH2:12][NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:4][C:5]2[O:10][CH2:9][CH2:8][CH2:7][C:6]=2[CH:11]=1참가 물질
실험 절차
A mixture of 6-hydroxy-3,4-dihydrobenzopyran-7-carboxaldehyde (429 mg, 2.41 mmol) and aniline (224 mg, 2.42 mmol) in methanol (30 mL) was warmed and the methanol, which distilled over, was collected. When 10 mL of methanol had been collected, the mixture was allowed to cool and the intermediate Schiff's base crystallized out. This material was collected and redissolved in fresh methanol (30 mL). Sodium borohydride (1 molar equiv.) was added in portions and the color immediately discharged. The mixture was concentrated to 50% of its original volume, then poured into an excess of water (100 mL). The aqueous solution was rendered acidic with 2N HCl, filtered to remove any insoluble material, then basified with 7%, NaHCO3. The product, which precipitated, was collected by filtration and dried to afford 6-hydroxy-7-phenylaminomethyl-3,4-dihydrobenzopyran (277 mg, 49%), m.p. 135°-137° C.
후처리
- temperaturewas warmed
- distillationthe methanol, which distilled over,
- customwas collected
- customWhen 10 mL of methanol had been collected
- temperatureto cool
- customthe intermediate Schiff's base crystallized out
- customThis material was collected
- dissolutionredissolved in fresh methanol (30 mL)
- additionSodium borohydride (1 molar equiv.) was added in portions
- concentrationThe mixture was concentrated to 50% of its original volume
- additionpoured into an excess of water (100 mL)
- filtrationfiltered
- customto remove any insoluble material
- customThe product, which precipitated
- filtrationwas collected by filtration
- customdried
출처 및 근거
- ORD 기록
- ord-e4122300dd304b1593bedf98eb030ac4
- 출처 데이터셋
- uspto-grants-1986_01
- 특허 번호
- US04563476
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