Methyl chloroformate → 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-yl Cloroformate

HRID 1902137Notes

Reaction equation

[CH3:1][O:2][N:3]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH:6]([OH:11])[CH2:5][C:4]1([CH3:13])[CH3:12].C[O:15][C:16]([Cl:18])=O>>[Cl:18][C:16]([O:11][CH:6]1[CH2:7][C:8]([CH3:9])([CH3:10])[N:3]([O:2][CH3:1])[C:4]([CH3:13])([CH3:12])[CH2:5]1)=[O:15]

Participants

Reactant 2

HCID 6586Methyl chloroformate

HCID 109977701-Methoxy-2,2,6,6-tetramethyl-piperidin-4-ol

Product 1

HCID 540353651-Methoxy-2,2,6,6-tetramethylpiperidin-4-yl Cloroformate

Procedure

The title compound is prepared by reacting 1-methoxy-2,2,6,6-tetramethylpiperidin-4-ol (1 mole) with methylchloroformate (1 mole).

Sources & evidence

ORD record: ord-40accf55a46840ab83fa589b43c91406
Source dataset: uspto-grants-1996_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05578731

Reaction notes

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