Acetic Acid → N-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amine

HRID 1024486

反応式

HRID 1024486 の反応式
[Cl:1][C:2]1[C:7]2[O:8][CH2:9][CH2:10][CH2:11][O:12][C:6]=2[CH:5]=[C:4]([CH:13]=O)[CH:3]=1.[CH2:15]([NH2:19])[CH:16]([CH3:18])[CH3:17].C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl>[Cl:1][C:2]1[C:7]2[O:8][CH2:9][CH2:10][CH2:11][O:12][C:6]=2[CH:5]=[C:4]([CH2:13][NH:19][CH2:15][CH:16]([CH3:18])[CH3:17])[CH:3]=1

参加物

6

反応物 4

HCID 176Acetic AcidHCID 6558IsobutylamineHCID 49622469-chloro-3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehydeHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 43087680N-(9-chloro-3,4-dihydro-2H-1,5-benzodioxepin-7-ylmethyl)-2-methylpropan-1-amine

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

To an ice cold mixture of 9-chloro-3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehyde (2.07 g) and of isobutylamine (7.5 ml 8 eq.) were combined in 1,2-dichloroethane (75 ml) and cooled in ice water bath. Acetic acid (5.68 ml) was then added and followed by sodium triacetoxyborohydride (2.75 g, 1.4 eq.). The mixture was allowed to stir at room temperature overnight. It was partitioned with aqueous K2CO3 (75 mL, 1.5M). The aqueous layer was extracted with of dichloromethane (75 ml×2). The organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by flash column chromatography (10-100% ethyl acetate in hexanes) gave the desired amine as a light yellow oil: MS (m+1)=270.2.

後処理

  1. customIt was partitioned with aqueous K2CO3 (75 mL, 1.5M)
  2. extractionThe aqueous layer was extracted with of dichloromethane (75 ml×2)
  3. washwashed with brine
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified by flash column chromatography (10-100% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-aec57fd526534ee0a281ac98e20cf341
出典データセット
uspto-grants-2014_05
特許番号
US08722896B2

関連ノート

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