反応 #4162685
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ec278794e22b49e6a0921689b46b256c表示可能な構造データがありません
CC(C(=O)OCC1=CC=CC=C1)O製品情報
benzyl 2-hydroxypropanoate (CAS 2051-96-9) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 98054
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ec278794e22b49e6a0921689b46b256c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d20cb56cf2534038bab7ed7a20c2dcc9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f6838e61a1b741879e2ef468db155d1b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-18d9f8f0df9d41318ab43f3a1d450cde反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ec278794e22b49e6a0921689b46b256c反応条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
ソース ID: ord-9f8135fc2ea3458ea13011035828fec5反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d20cb56cf2534038bab7ed7a20c2dcc9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f6838e61a1b741879e2ef468db155d1b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-18d9f8f0df9d41318ab43f3a1d450cde反応条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
ソース ID: ord-9f8135fc2ea3458ea13011035828fec5反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reaction Scheme A above begins with the triflate of a carboxyl-protected D-αhydroxycarboxylic acid derivative, e.g., lactic acid benzyl ester. By reacting this triflate with α-ethyl-γ-anilido-L-glutamate (prepared, for example, by reacting an amino-protected L-glutamic acid, such as Nα -Cbo-L-glutamic acid, with diethyl sulfate in triethylamine and dichloromethane at room temperature for about three days to give Nα -Cbo-α-ethyl-L-glutamate, forming the dicyclohexylamine salt of the thus-obtained glutamate by reaction with dicyclohexylamine in ethyl acetate at room temperature overnight, acidifying a suspension of the dicyclohexylamine salt and then reacting the isolated free acid with dicyclohexylcarbodiimide and aniline in dichloromethane, first in a dry ice/ice/acetone bath for one hour, and then at room temperature overnight), Nα -[1(L)-carbethoxy-3-carboxanilidopropyl]-L alanine benzyl ester is obtained. Reaction Scheme A
ソース ID: ord-e9b05a6d4a554cc5bf3c38bb7c250d78反応条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Construction of Benzyl-L-lactic Acid. L-Lactic acid (9 g, 100 mmol) is added to N,N'-diisopropylbenzylisourea (23.3 g, 100 mmol) with stirring. The mixture becomes very viscous within 10 min and is stirred intermittently for 1 h. The volume is then increased to 200 mL with THF, and the mixture stirred for 48 h at room temperature. After cooling the mixture to -15° C., the diisopropylurea is removed by filtration and the THF is evaporated under reduced pressure. The resulting thick oil is pumped under high vacuum for 24 h to give benzyl lactate (17.4 g, 95%) which may be used without further purification. is stirred intermittently for 1 h the mixture stirred for 48 h at room temperature the diisopropylurea is removed by filtration the THF is evaporated under reduced pressure The resulting thick oil is pumped under high vacuum for 24 h
ソース ID: ord-ac871ceb01844d57beddf303b82b968dPubChem References
化合物の公開データベース記録に掲載された情報源です。
