Isopropyl chloroformate → HCID 86754732, compound

HRID 1600512Notes

Reaction equation

[CH:1]#[C:2][C:3]1[CH:8]=[CH:7][C:6]([OH:9])=[CH:5][CH:4]=1.[C:10](Cl)(=[O:15])[O:11][CH:12]([CH3:14])[CH3:13]>>[CH:12]([O:11][C:10]([O:9][C:6]1[CH:7]=[CH:8][C:3]([CH:2]=[CH2:1])=[CH:4][CH:5]=1)=[O:15])([CH3:14])[CH3:13].[OH:9][C:6]1[CH:7]=[CH:8][C:3]([CH:2]=[CH2:1])=[CH:4][CH:5]=1

Participants

Reactant 2

HCID 7917Isopropyl chloroformate

HCID 327584-Ethynylphenol

Product 1

HCID 86754732HCID 86754732, compound

Procedure

Using 12.0 g of poly(p-hydroxystyrene) obtained according to (2) above and 3.0 g of isopropyl chlorocarbonate, reaction and after-treatments were carried out according to (2) of Preparation Example 6 to obtain 11.7 g of poly(p-isopropoxycarbonyloxystyrene/p-hydroxystyrene) as white powdery crystal. P-isopropoxycarbonyloxystyrene unit/p-hydorxystyrene unit molar ratio in the polymer≈2:8 (1H NMR). Mw≈8,000; Mw/Mn=1.60 (GPC with polystyrene calibration).

Workup

customobtained

Sources & evidence

ORD record: ord-11e91ed68e5d483ca9a981cff7f2ef93
Source dataset: uspto-grants-1999_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05976759

Reaction notes

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