4-Hydroxybenzyl Alcohol → HCID 22279993, compound

HRID 1063721Notes

Reaction equation

HRID 1063721 reaction equation
C[O:2][C:3](=[O:16])[CH2:4][O:5][C:6]1[CH:14]=[CH:13][C:12]([SH:15])=[C:11]2[C:7]=1[CH2:8][CH2:9][CH2:10]2.[CH2:17]([O:24][C:25]1[CH:30]=[CH:29][C:28]([CH2:31]Cl)=[CH:27][CH:26]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.OCC1C=CC(O)=CC=1.BrCC1C=CC=CC=1.ClCC1(C(F)(F)F)C=CC(OCC2C=CC=CC=2)=CC1>>[CH2:17]([O:24][C:25]1[CH:26]=[CH:27][C:28]([CH2:31][S:15][C:12]2[CH:13]=[CH:14][C:6]([O:5][CH2:4][C:3]([OH:2])=[O:16])=[C:7]3[C:11]=2[CH2:10][CH2:9][CH2:8]3)=[CH:29][CH:30]=1)[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1

Participants

6

Reactant 5

HCID 1254-Hydroxybenzyl AlcoholHCID 7498Benzyl BromideHCID 700424-Benzyloxybenzyl chlorideHCID 20770872(7-Mercapto-indan-4-yloxy)-acetic Acid Methyl EsterHCID 694705984-Chloromethyl-(4-trifluoromethyl-benzyloxy-benzene)

Product 1

HCID 22279993HCID 22279993, compound

Procedure

The title compound was prepared in the manner analogous to Example 1F using 12C and 1-benzyloxy-4-chloromethyl-benzene prepared from 4-hydroxymethyl-phenol and 4-bromomethyl-benzene in the manner analagous to Examples 14A and 14B. MS m/z 435 (M+1).

Sources & evidence

ORD record
ord-b6a4addddf2a4cd9beba9c25f260da25
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

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