Neopentyl glycol → HCID 20324843, compound

HRID 838845Notes

Reaction equation

HRID 838845 reaction equation
[C:1]([C:6]1[CH:7]=[C:8]([CH:17]=[C:18]([C:21]([CH2:24]C)([CH3:23])[CH3:22])[C:19]=1[OH:20])[CH2:9][P:10]1(=[O:16])[O:14][CH2:13][CH:12](C)[O:11]1)([CH2:4]C)([CH3:3])[CH3:2].CC(C)(CO)CO.C(C1C=C(C=C(C(CC)(C)C)C=1O)CP(=O)(OC1C=CC=CC=1)OC1C=CC=CC=1)(CC)(C)C.C(C1C=C(C=C(C(C)(C)C)C=1O)CP(=O)(OC1C=CC=CC=1)OC1C=CC=CC=1)(C)(C)C>>[C:21]([C:18]1[CH:17]=[C:8]([CH:7]=[C:6]([C:1]([CH3:4])([CH3:3])[CH3:2])[C:19]=1[OH:20])[CH2:9][P:10]1(=[O:16])[O:11][CH2:12][CH2:13][O:14]1)([CH3:24])([CH3:23])[CH3:22]

Participants

5

Reactant 4

HCID 31344Neopentyl glycolHCID 13651368HCID 13651368, compoundHCID 20324838HCID 20324838, compoundHCID 20324846HCID 20324846, compound

Product 1

HCID 20324843HCID 20324843, compound

Procedure

Similarly, 1-(3,5-di-tert-amyl-4-hydroxybenzyl)-3-methyl-1-oxo-2,5-dioxa-1-phosphacyclopentane is made by substituting 1,2-propanediol for 2,2-dimethyl-1,3-propanediol and diphenyl 3,5-di-tert-amyl-4-hydroxybenzylphosphonate for diphenyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate in Example 2.

Sources & evidence

ORD record
ord-674d8b2e2259488db77f226ba3fe09c9
Source dataset
uspto-grants-1978_06
Patent number
US04093588

Reaction notes

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