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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908567Generated: October 27, 2026

Chloroacetaldehyde → HCID 59129491, compound

https://huagongshe.com/reaction/1908567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59129217HCID 59129217—
SolventDichloromethaneHCID 6344—
ProductHCID 59129491HCID 5912949163%

Reaction Steps

To a solution of N-(2-tert-butyl-1-(2-cyanoethyl)indolin-5-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide (71 mg, 0.17 mmol) in anhydrous dichloromethane (1 mL) was added chloroacetaldehyde (53 μL, 0.41 mmol) at room temperature under N2. After 20 min of stirring, NaBH(OAc)3 (90 mg, 0.42 mmol) was added in two portions. The reaction mixture was stirred overnight at room temperature. The product was purified by column chromatography on silica gel (2-15% ethyl acetate/hexanes) providing N-(2-tert-butyl-1-(2-chloroethyl)indolin-5-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide (51 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-dc4dd6115bcd4220ab2487632374a5c6
Source noteuspto-grants-2013_12