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Formic Acid → HCID 86744910、化合物

HRID 1086801
ノート
印刷プレビュー

反応式

HRID 1086801 の反応式
N(C(OCC)=O)=N[C:3](OCC)=[O:4].[OH:13][C@@H:14]1[CH2:18][CH2:17][C@H:16]([NH:19][C:20](=[O:29])[O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:15]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(O)=O>C1COCC1.CCOCC.C1CCCCC1>[CH:3]([O:13][C@H:14]1[CH2:18][CH2:17][C@H:16]([NH:19][C:20](=[O:29])[O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)[CH2:15]1)=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 284Formic AcidHCID 11776TriphenylphosphineHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 86331931benzyl N-[(1S,3R)-rel-3-hydroxycyclopentyl]carbamate

生成物 1

HCID 86744910HCID 86744910、化合物収率 88.6%

試薬・触媒・溶媒 3

HCID 3283
Diethyl Ether
溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8078Cyclohexane溶媒

実験手順

Diethyl azodicarboxylate (1.78 g) was added dropwise to a stirred solution of N-(cis-3-hydroxycyclopentyl)carbamic acid, (phenylmethyl) ester (1.19 g), triphenylphosphine (2.68 g) and formic acid (0.47 g) in THF (65 ml) under nitrogen at room temperature. The resulting solution was stirred for 2 h, and concentrated to give a residue which was stirred in ether (20 ml) at ca -10° under nitrogen for 1 h. The mixture was diluted with cyclohexane (20 ml), and the solid was filtered off and washed with ether:cyclohexane (1:1; 3×ca. 20 ml). The combined filtrate and washings were concentrated, and the resultant residue was purified by FCC eluting with ethyl acetate:cyclohexane (2:3) to give the title compound (1.18 g), m.p. 45°-48°.

後処理

  1. concentrationconcentrated
  2. customto give a residue which
  3. filtrationthe solid was filtered off
  4. washwashed with ether:cyclohexane (1:1; 3×ca. 20 ml)
  5. concentrationThe combined filtrate and washings were concentrated
  6. customthe resultant residue was purified by FCC
  7. washeluting with ethyl acetate:cyclohexane (2:3)

出典と根拠

ORDレコード
ord-ab8f1073898b4d2f92c175e127286fac
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05032583

反応ノート

読み込み中…

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