HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Benzyloxy-alpha,alpha,alpha',alpha'tetramethyl-1,3-benzenedimethanol → 3,5-Dibenzhydrylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Benzyloxy-alpha,alpha,alpha',alpha'tetramethyl-1,3-benzenedimethanol | HCID 9922370 | — |
| Reactant | 5Benzyloxy-alpha,alpha, alpha',alpha'-tetraphenyl-1,3-benzenedimethanol | HCID 22660338 | — |
| Product | 3,5-Dibenzhydrylphenol | HCID 22660342 | — |
Reaction Steps
The procedure (including reaction and treatment) of Example 2 was repeated, except that 5-benzyloxy-α,α,α′,α′-tetramethyl-1,3-benzenedimethanol was replaced by 5benzyloxy-α,α, α′,α′-tetraphenyl-1,3-benzenedimethanol, to thereby yield the above-described target as a colorless oil. IR(film)cm−1: 3536, 3410, 3061, 3026, 1597, 1494. 1H-NMR(CDCl3)δ: 4.52(1H,br.s), 5.40(2H,s), 6.37(2H,s), 6.57(1H,s), 7.05(8H,dd,J=8.3,1.5 Hz), 7.15-7.26(12H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806395B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-d563082eddca42b5886f1313f7874d2d |
| Source note | uspto-grants-2004_10 |