(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

Base Information

Chemical Name:(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester
CAS No.:497830-76-9
Molecular Formula:C₂₆H₂₉NO₅
Molecular Weight:435.52
Hs Code.:

Synonyms:(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

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Chemical Property of (3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

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Technology Process of (3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

There total 7 articles about (3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester 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: 63.0%

: 497830-86-1
(E)-(R)-4-[Benzyl-((E)-4-oxo-pent-2-enoyl)-amino]-5-benzyloxy-pent-2-enoic acid ethyl ester

: 497830-76-9
(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

Guidance literature:: In toluene; at 110 ℃;
DOI:10.1016/S0040-4039(02)01711-2

Reference yield:

: 79069-54-8
(S)-2-(t-butoxycarbonylamino)-3-phenylmetoxy-1-propanal

: 497830-76-9
(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: potassium tert-butylate / tetrahydrofuran

2: trifluoroacetic acid / 20 °C

3: CsCO₃ / dichloromethane

4: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / 0 °C

5: toluene / 110 °C

With 1-hydroxy-7-aza-benzotriazole; potassium tert-butylate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene; 5: intramolecular Diels-Alder reaction;
DOI:10.1016/S0040-4039(02)01711-2

Reference yield:

: 115186-34-0
tert-butyl ((S)-3-(benzyloxy)-1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate

: 497830-76-9
(3R,3aR,4S,7aR)-2-Benzyl-3-benzyloxymethyl-6-methyl-1-oxo-1,2,3,3a,4,7a-hexahydro-pyrano[3,4-c]pyrrole-4-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / -78 °C

2: potassium tert-butylate / tetrahydrofuran

3: trifluoroacetic acid / 20 °C

4: CsCO₃ / dichloromethane

5: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / 0 °C

6: toluene / 110 °C

With lithium aluminium tetrahydride; 1-hydroxy-7-aza-benzotriazole; potassium tert-butylate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene; 6: intramolecular Diels-Alder reaction;
DOI:10.1016/S0040-4039(02)01711-2