2-(2-(2-Chloroethoxy)ethoxy)ethanol → HCID 13859708, compound
Reaction equation
C(CC[S:22][CH2:23][CH2:24][O:25][CH2:26][CH2:27][O:28][CH2:29][CH2:30][OH:31])(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F.[C:32]([CH2:51][CH2:52][S:53][CH2:54][CH2:55]OCCS)([C:35]([C:38]([C:41]([C:44]([C:47]([F:50])([F:49])[F:48])([F:46])[F:45])([F:43])[F:42])([F:40])[F:39])([F:37])[F:36])([F:34])[F:33].ClCCOCCOCCO>>[C:32]([CH2:51][CH2:52][S:53][CH2:54][CH2:55][S:22][CH2:23][CH2:24][O:25][CH2:26][CH2:27][O:28][CH2:29][CH2:30][OH:31])([C:35]([C:38]([C:41]([C:44]([C:47]([F:48])([F:49])[F:50])([F:45])[F:46])([F:43])[F:42])([F:40])[F:39])([F:37])[F:36])([F:34])[F:33]Participants
4
Procedure
By proceeding in the same manner, C6F13C2H4S(C2H4O)3H is prepared from C6F13C2H4SC2H4OC2H4SH and Cl(C2H4O)3H.
Sources & evidence
- ORD record
- ord-964e08d6ff75486fa324a91d097d22a9
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04859797
Reaction notes
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