tert-butyl N-(2-hydroxyethyl)carbamate → HCID 19596665, compound

HRID 612888Notes

Reaction equation

HRID 612888 reaction equation
[OH:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[CH3:13])[O:4][N:3]=1.[C:14]([O:18][C:19]([NH:21][CH2:22][CH2:23]O)=[O:20])([CH3:17])([CH3:16])[CH3:15]>>[C:14]([O:18][C:19]([NH:21][CH2:22][CH2:23][O:1][C:2]1[CH:6]=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[CH3:13])[O:4][N:3]=1)=[O:20])([CH3:17])([CH3:16])[CH3:15]

Participants

3

Reactant 2

HCID 2733206tert-butyl N-(2-hydroxyethyl)carbamateHCID 178424181HCID 178424181, compound

Product 1

HCID 19596665HCID 19596665, compoundYield 86%

Procedure

3-Hydroxy-5-(2-methylphenyl)isoxazole (0.2 g) and 2-(N-tert-butoxycarbonylamino)ethanol (0.2 g) were subjected to reaction and post-treatment in a similar manner to that described in Example 9(a) to obtain the title compound (0.31 g, 86%) as a colorless powder.

Sources & evidence

ORD record
ord-34f6b64bca8a4d2393875fbe2927e1cd
Source dataset
uspto-grants-1999_12
Patent number
US06005116

Reaction notes

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