Chloroform → HCID 14478581, compound
Reaction equation
[C:1]([C@@:3]1([CH3:17])[CH2:8][CH2:7][C:6]2[C:9]([CH3:16])=[C:10]([OH:15])[C:11]([CH3:14])=[C:12]([CH3:13])[C:5]=2[O:4]1)#[CH:2].[CH:18](Cl)(Cl)Cl>>[C:1]([C@@:3]1([CH3:17])[CH2:8][CH2:7][C:6]2[C:9]([CH3:16])=[C:10]([O:15][CH3:18])[C:11]([CH3:14])=[C:12]([CH3:13])[C:5]=2[O:4]1)#[CH:2]Participants
3
Procedure
By the same procedure as described in Example 28 (R)-2-ethynyl-3,4-dihydro-6-methoxy-,5,7,8-tetramethyl-H-1-benzopyran was prepared from (R)-(-)-2-ethynyl-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-6-ol. This product was produced as white prisms=93°-95° C. [α]D25 -57.14°, (C 0.28, CHCl3).
Sources & evidence
- ORD record
- ord-1cde49e894b941dca8c8c47eeaa6ebb9
- Source dataset
- uspto-grants-1990_02
- Patent number
- US04898953
Reaction notes
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