Furfural diethyl acetal → HCID 15434861, compound

HRID 1604456

Reaction equation

HRID 1604456 reaction equation
[CH2:1]([O:3][CH:4]([O:23][CH2:24][CH3:25])[C:5]1S[C:7]([Sn:10]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:11][CH2:12][CH2:13][CH3:14])=[CH:8][CH:9]=1)[CH3:2].C([O:28]C(OCC)C1OC=CC=1)C>>[CH2:1]([O:3][CH:4]([O:23][CH2:24][CH3:25])[C:5]1[O:28][C:7]([Sn:10]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:11][CH2:12][CH2:13][CH3:14])=[CH:8][CH:9]=1)[CH3:2]

Participants

3

Reactant 2

HCID 83553Furfural diethyl acetalHCID 15434854HCID 15434854, compound

Product 1

HCID 15434861HCID 15434861, compoundYield 82%

Procedure

Following the procedure for preparing 2-(diethoxymethyl)-5-(tributylstannyl)-thiophene as described in step (1) of Example 1, 17 g (10 mmol) of 2-(diethoxymethyl)furan was converted to 32.6 g (82% yield) of 2-(diethoxymethyl)-5-(tributylstannyl) furan (bp 110° C., 1 torr).

Sources & evidence

ORD record
ord-05e3189ee62643b59d248db4b713fd4b
Source dataset
uspto-grants-1999_11
Patent number
US05994394

Linked notes

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