Ethyl bromoacetate → HCID 53885943, compound

HRID 1449069Notes

Reaction equation

Br[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[CH2:8]([C:10]1([CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH2:19][C:18]2[C:13](=[C:14]([O:22]CC3C=CC=CC=3)[CH:15]=[C:16]([CH:20]=O)[CH:17]=2)[C:12](=[O:30])[CH2:11]1)[CH3:9]>>[CH2:8]([C:10]1([CH2:31][C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)[CH2:19][C:18]2[C:13](=[C:14]([OH:22])[CH:15]=[C:16]([CH2:20][CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4])[CH:17]=2)[C:12](=[O:30])[CH2:11]1)[CH3:9]

Participants

Reactant 2

HCID 7748Ethyl bromoacetate

HCID 20531466HCID 20531466, compound

Product 1

HCID 53885943HCID 53885943, compound

Procedure

Ethyl bromoacetate is converted to the triphenyl phosphorone, reacted with the product of Example 36 and reduced catalytically to the desired compound using procedures analogous to those described in Example 24.

Sources & evidence

ORD record: ord-0e41f090c9cd4e839698c01949a81ec9
Source dataset: uspto-grants-1980_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04188495

Reaction notes

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