Methyl cyclopentanecarboxylate → HCID 19920119, compound

HRID 1648485Notes

Reaction equation

[CH:1]1([C:6]([O:8][CH3:9])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:10][O:11][CH:12]([O:16][CH3:17])[CH2:13][CH2:14]Br>>[CH3:10][O:11][CH:12]([O:16][CH3:17])[CH2:13][CH2:14][C:1]1([C:6]([O:8][CH3:9])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

Reactant 2

HCID 78365Methyl cyclopentanecarboxylate

HCID 1189323-Bromopropionaldehyde dimethylacetal

Product 1

HCID 19920119HCID 19920119, compoundYield 72%

Procedure

Prepared according to a procedure identical to Stage A of Example 6, starting from methyl cyclopentanecarboxylate and 3-bromopropionaldehyde dimethyl acetal, with a 72% yield.

Workup

customPrepared

Sources & evidence

ORD record: ord-ba9f1abd60db43eb871d8160da0eecbc
Source dataset: uspto-grants-1995_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05436343

Reaction notes

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