Chloroform → HCID 53642313, compound
Reaction equation
[CH3:1][C@:2]1([CH2:16][CH2:17]O)[CH2:11][CH2:10][C:9]2[C:4](=[C:5]([CH3:15])[C:6]([CH3:14])=[C:7]([OH:13])[C:8]=2[CH3:12])[O:3]1.C(Cl)(Cl)[Cl:20]>>[CH3:1][C@:2]1([CH2:16][CH2:17][Cl:20])[CH2:11][CH2:10][C:9]2[C:4](=[C:5]([CH3:15])[C:6]([CH3:14])=[C:7]([OH:13])[C:8]=2[CH3:12])[O:3]1Participants
3
Procedure
(R)-2,5,7,8-tetramethyl-6-hydroxy-2-(2-chloroethyl)-chroman was prepared from (R)-2,5,7,8-tetramethyl-6-hydroxy-2-(2-hydroxyethyl)-chroman by a procedure similar to that described in Example 10. [α]D20 =+9.0, (c=2, chloroform), mp.=111° C.
Sources & evidence
- ORD record
- ord-f8e47bfb32214becbdabc611d9425803
- Source dataset
- uspto-grants-1987_02
- Patent number
- US04645845
Reaction notes
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