ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

Base Information

Chemical Name:ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate
CAS No.:1201815-22-6
Molecular Formula:C₁₄H₂₅NO₆
Molecular Weight:303.356
Hs Code.:

Synonyms:ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

Suppliers and Price of ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

There total 1 articles about ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate 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: 85.0%

: 1201815-21-5
ethyl (1R,2R)-2-tert-butoxycarbonylaminocyclohex-4-enecarboxylate

: 1201815-22-6
ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

Guidance literature:: ethyl (1R,2R)-2-tert-butoxycarbonylaminocyclohex-4-enecarboxylate; With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In acetone; tert-butyl alcohol; at 20 ℃; for 4h;

With water; sodium sulfite; In acetone; tert-butyl alcohol; diastereoselective reaction;
DOI:10.1016/j.tetasy.2009.09.001

Reference yield: 77.0%

: 1201815-22-6
ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

: 1129973-34-7
(1R,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid

Guidance literature:: With water; at 150 ℃; for 1h; Microwave irradiation;
DOI:10.1016/j.tetasy.2009.09.001

Reference yield: 45.0%

: 1201815-22-6
ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate

: 1201815-29-3
(1R,2R,4R,5S)-2-amino-4,5-dihydroxycyclohexanecarboxylic acid hydrochloride

Guidance literature:: ethyl (1R,2R,4R,5S)-2-tert-butoxycarbonylamino-4,5-dihydroxycyclohexanecarboxylate; With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 5h;

With hydrogenchloride; In water; for 24h; Reflux;
DOI:10.1016/j.tetasy.2009.09.001