methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

Base Information

Chemical Name:methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate
CAS No.:904682-02-6
Molecular Formula:C₁₈H₂₁NO₅
Molecular Weight:331.368
Hs Code.:

Synonyms:methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

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Chemical Property of methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

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Technology Process of methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

There total 3 articles about methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 904681-97-6
methyl (2Z)-2-{[(benzyloxy)carbonyl]amino}-3-(5-ethyl-2-furyl)acrylate

: 904682-02-6
methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

: methyl (2S)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

Guidance literature:: With hydrogen; di(norbornadiene)rhodium(I) tetrafluoroborate; In methanol; toluene; at 20 ℃; for 17.5h; under 3750.38 Torr; Title compound not separated from byproducts.;
DOI:10.1002/chem.200600192

Reference yield:

: 23074-10-4
5-ethylfurfural

: 904682-02-6
methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / t-BuOK / CH₂Cl₂ / 2 h / 20 °C

2: MandyPhos(OMe); H₂ / [Rh(nbd)2]BF₄ / methanol; toluene / 17.5 h / 20 °C / 3750.38 Torr

With potassium tert-butylate; hydrogen; di(norbornadiene)rhodium(I) tetrafluoroborate; In methanol; dichloromethane; toluene; 1: Horner-Wadsworth-Emmons reaction;
DOI:10.1002/chem.200600192

Reference yield:

: 100945-15-1,88568-95-0
N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester

: 904682-02-6
methyl (2R)-(-)-2-benzyloxycarbonylamino-3-(5-ethylfuran-2-yl)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / t-BuOK / CH₂Cl₂ / 2 h / 20 °C

2: MandyPhos(OMe); H₂ / [Rh(nbd)2]BF₄ / methanol; toluene / 17.5 h / 20 °C / 3750.38 Torr

With potassium tert-butylate; hydrogen; di(norbornadiene)rhodium(I) tetrafluoroborate; In methanol; dichloromethane; toluene; 1: Horner-Wadsworth-Emmons reaction;
DOI:10.1002/chem.200600192