Benzyl Alcohol → Benzyl [1-(4-nitrobenzyl)but-3-enyl]carbamate

HRID 1584756ノート

反応式

HRID 1584756 の反応式
[N+:1]([C:4]1[CH:17]=[CH:16][C:7]([CH2:8][CH:9]([CH2:13][CH:14]=[CH2:15])C(O)=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:25])C=CC=CC=1.C([N:37]([CH2:40]C)CC)C.[CH2:42]([OH:49])[C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1>C1(C)C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([CH2:8][CH:9]([NH:37][C:40](=[O:25])[O:49][CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=2)[CH2:13][CH:14]=[CH2:15])=[CH:16][CH:17]=1)([O-:3])=[O:2]

参加物

6

反応物 4

HCID 244Benzyl AlcoholHCID 8471TriethylamineHCID 199401P,P-Diphenylphosphinic azideHCID 224570092-(4-Nitrobenzyl)pent-4-enoic acid

生成物 1

HCID 53992691Benzyl [1-(4-nitrobenzyl)but-3-enyl]carbamate

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

2-(4-Nitrobenzyl)pent-4-enoic acid (9.3 g, 40.0 mmol) is treated in toluene with 11.55 g (42.0 mmol) of diphenylphosphoryl azide at 50° C. in the presence of triethylamine (5.6 ml, 40.0 mmol) and benzyl alcohol (5.18 g, 48.0 mmol). After 20 minutes, the temperature is slowly increased and the mixture is then boiled under reflux for a further 3 hours. After cooling, the reaction mixture is washed twice with 1N sodium hydroxide solution, twice with 1N hydrochloric acid and twice with brine, dried over sodium sulfate and evaporated on a rotary evaporator. The title compound is obtained as white crystals after crystallization of the crude product from toluene/hexane. M.p.: 94-95° C. TLC: ethyl acetate/hexane (1:3) Rf =0.22.

後処理

  1. temperaturethe temperature is slowly increased
  2. temperatureunder reflux for a further 3 hours
  3. temperatureAfter cooling
  4. washthe reaction mixture is washed twice with 1N sodium hydroxide solution, twice with 1N hydrochloric acid and twice with brine
  5. dry with materialdried over sodium sulfate
  6. customevaporated on a rotary evaporator

出典と根拠

ORDレコード
ord-e246c553bc4848909cce11fb2dac40dd
出典データセット
uspto-grants-1999_08
特許番号
US05935951

反応ノート

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