HCID 14834980, compound → HCID 14834981, compound

HRID 846982Notes

Reaction equation

COC([NH:5][CH:6]([CH2:9][O:10][C:11](=[O:31])[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:7][OH:8])=O.[C:32]([O:36][C:37]([O:39]C([O-])=O)=O)([CH3:35])([CH3:34])[CH3:33]>>[C:32]([O:36][C:37]([NH:5][CH:6]([CH2:9][O:10][C:11](=[O:31])[NH:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH3:30])[CH2:7][OH:8])=[O:39])([CH3:33])([CH3:34])[CH3:35]

Participants

Reactant 2

HCID 14834980HCID 14834980, compound

HCID 22064466Tert-butyldicarbonate

Product 1

HCID 14834981HCID 14834981, compoundYield 93.4%

Procedure

2-tert-Butoxycarbonylamino-3-octadecylcarbamoyloxypropanol V e2 is prepared by the same manner as described in (41) by using tert-butyldicarbonate instead of methyl chloroformate.

Sources & evidence

ORD record: ord-8d50303a6fec43c48c364f57262345c3
Source dataset: uspto-grants-1992_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05138067

Reaction notes

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